New CACNA1A deletions are associated to migraine phenotypes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1129-2377

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: New CACNA1A deletions are associated to migraine phenotypes ; volume:19 ; number:1 ; day:30 ; month:8 ; year:2018 ; pages:1-6 ; date:12.2018
The journal of headache and pain ; 19, Heft 1 (30.8.2018), 1-6, 12.2018

Creator: Grieco, G. S.

Contributor: Gagliardi, S.
Ricca, I.
Pansarasa, O.
Neri, M.
Gualandi, F.
Nappi, G.
Ferlini, A.
Cereda, C.
SpringerLink (Online service)

DOI: 10.1186/s10194-018-0891-x

URN: urn:nbn:de:101:1-2018102023452864366151

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:20 AM CEST

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Grieco, G. S.
Gagliardi, S.
Ricca, I.
Pansarasa, O.
Neri, M.
Gualandi, F.
Nappi, G.
Ferlini, A.
Cereda, C.
SpringerLink (Online service)

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Unveiling nonessential gene deletions that confer significant morphological phenotypes beyond natural yeast strains

FGF-21 and GDF-15 are increased in migraine and associated with the severity of migraine-related disability

Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

CDKN2A/B deletions are strongly associated with meningioma progression: a meta-analysis of individual patient data

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints

Clinical phenotypes of MAGEL2 mutations and deletions

Deletions of chromosomal regulatory boundaries are associated with congenital disease

Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure

Terminal 18q deletions are stabilized by neotelomeres

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Multiple loci are associated with white blood cell phenotypes

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Unveiling nonessential gene deletions that confer significant morphological phenotypes beyond natural yeast strains

FGF-21 and GDF-15 are increased in migraine and associated with the severity of migraine-related disability

Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

CDKN2A/B deletions are strongly associated with meningioma progression: a meta-analysis of individual patient data

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints

Clinical phenotypes of MAGEL2 mutations and deletions

Deletions of chromosomal regulatory boundaries are associated with congenital disease

Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure

Terminal 18q deletions are stabilized by neotelomeres

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Multiple loci are associated with white blood cell phenotypes

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Unveiling nonessential gene deletions that confer significant morphological phenotypes beyond natural yeast strains

FGF-21 and GDF-15 are increased in migraine and associated with the severity of migraine-related disability

Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

CDKN2A/B deletions are strongly associated with meningioma progression: a meta-analysis of individual patient data

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints

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New CACNA1A deletions are associated to migraine phenotypes

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Other Objects (12)

Clinical phenotypes of MAGEL2 mutations and deletions

Deletions of chromosomal regulatory boundaries are associated with congenital disease

Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure

Terminal 18q deletions are stabilized by neotelomeres

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Multiple loci are associated with white blood cell phenotypes

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Unveiling nonessential gene deletions that confer significant morphological phenotypes beyond natural yeast strains

FGF-21 and GDF-15 are increased in migraine and associated with the severity of migraine-related disability

Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

CDKN2A/B deletions are strongly associated with meningioma progression: a meta-analysis of individual patient data

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints

Clinical phenotypes of MAGEL2 mutations and deletions

Deletions of chromosomal regulatory boundaries are associated with congenital disease

Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure

Terminal 18q deletions are stabilized by neotelomeres

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Multiple loci are associated with white blood cell phenotypes

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Unveiling nonessential gene deletions that confer significant morphological phenotypes beyond natural yeast strains

FGF-21 and GDF-15 are increased in migraine and associated with the severity of migraine-related disability

Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

CDKN2A/B deletions are strongly associated with meningioma progression: a meta-analysis of individual patient data

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints

Clinical phenotypes of MAGEL2 mutations and deletions

Deletions of chromosomal regulatory boundaries are associated with congenital disease

Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure

Terminal 18q deletions are stabilized by neotelomeres

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Multiple loci are associated with white blood cell phenotypes

Different pain phenotypes are associated with anti-Caspr2 autoantibodies

Unveiling nonessential gene deletions that confer significant morphological phenotypes beyond natural yeast strains

FGF-21 and GDF-15 are increased in migraine and associated with the severity of migraine-related disability

Local and global chromatin interactions are altered by large genomic deletions associated with human brain development

CDKN2A/B deletions are strongly associated with meningioma progression: a meta-analysis of individual patient data

Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3′ Breakpoints

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