Elucidating the molecular genetic basis of cluster headache: delineation of the genetic architecture by exome sequencing
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1129-2377
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Elucidating the molecular genetic basis of cluster headache: delineation of the genetic architecture by exome sequencing ; volume:14 ; number:1 ; day:21 ; month:2 ; year:2013 ; pages:1 ; date:2.2013
The journal of headache and pain ; 14, Heft 1 (21.2.2013), 1, 2.2013
- Classification
-
Medizin, Gesundheit
- Creator
-
Southgate, L.
Scollen, S.
He, W.
Moss, A.
Simpson, MA
Zhang, B.
Xi, L.
Schlitt, T.
Weale, ME
Hyde, CL
Stephens, JC
Sjöstrand, C.
Russell, MB
Leone, M.
John, SL
Trembath, RC
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/1129-2377-14-S1-P34
- URN
-
urn:nbn:de:101:1-2019060905305464659193
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:00 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Southgate, L.
- Scollen, S.
- He, W.
- Moss, A.
- Simpson, MA
- Zhang, B.
- Xi, L.
- Schlitt, T.
- Weale, ME
- Hyde, CL
- Stephens, JC
- Sjöstrand, C.
- Russell, MB
- Leone, M.
- John, SL
- Trembath, RC
- SpringerLink (Online service)
Other Objects (12)
Elucidating the mechanisms underlying Alzheimer's disease-associated genetic polymorphisms
Elucidating the genetic basis of social interaction and isolation
Identification of functional genetic variation in exome sequence analysis
Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity
Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Elucidating the genetic basis and molecular mechanisms of dioecy in Populus
Exome scale map of genetic alterations promoting metastasis in colorectal cancer
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Exome-based investigation of the genetic basis of human pigmentary glaucoma
Exome-assistant: a rapid and easy detection of disease-related genes and genetic variations from exome sequencing
Elucidating the mechanisms underlying Alzheimer's disease-associated genetic polymorphisms
Elucidating the genetic basis of social interaction and isolation
Identification of functional genetic variation in exome sequence analysis
Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity
Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Elucidating the genetic basis and molecular mechanisms of dioecy in Populus
Exome scale map of genetic alterations promoting metastasis in colorectal cancer
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Exome-based investigation of the genetic basis of human pigmentary glaucoma
Exome-assistant: a rapid and easy detection of disease-related genes and genetic variations from exome sequencing
Elucidating the mechanisms underlying Alzheimer's disease-associated genetic polymorphisms
Elucidating the genetic basis of social interaction and isolation
Identification of functional genetic variation in exome sequence analysis
Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
Targeted exome sequencing for mitochondrial disorders reveals high genetic heterogeneity
Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Elucidating the genetic basis and molecular mechanisms of dioecy in Populus
Exome scale map of genetic alterations promoting metastasis in colorectal cancer
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Exome-based investigation of the genetic basis of human pigmentary glaucoma