- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1710-1492
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
X-linked SCID with a rare mutation ; volume:17 ; number:1 ; day:11 ; month:10 ; year:2021 ; pages:1-9 ; date:12.2021
Allergy, asthma and clinical immunology ; 17, Heft 1 (11.10.2021), 1-9, 12.2021
- Creator
-
Mahdavi, Fatemeh Sadat
Keramatipour, Mohammad
Ansari, Sarina
Sharafian, Samin
Karamzade, Arezou
Tavakol, Marzieh
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13223-021-00605-7
- URN
-
urn:nbn:de:101:1-2021122608590294230315
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:29 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
- Mahdavi, Fatemeh Sadat
- Keramatipour, Mohammad
- Ansari, Sarina
- Sharafian, Samin
- Karamzade, Arezou
- Tavakol, Marzieh
- SpringerLink (Online service)
Other Objects (12)
X-linked dominant RPGR gene mutation in a familial Coats angiomatosis
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family
The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease
X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
X-linked disorders with cerebellar dysgenesis
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family
X-linked Hyper-IgM Syndrome with Bronchiectasis
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
X-linked dominant RPGR gene mutation in a familial Coats angiomatosis
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family
The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease
X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
X-linked disorders with cerebellar dysgenesis
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family
X-linked Hyper-IgM Syndrome with Bronchiectasis
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
Molecular genetic mechanisms surrounding x-linked Dystonia-Parkinsonism
X-linked dominant RPGR gene mutation in a familial Coats angiomatosis
Easily misdiagnosed X-linked adrenoleukodystrophy
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family
The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease
X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
X-linked disorders with cerebellar dysgenesis
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family
X-linked Hyper-IgM Syndrome with Bronchiectasis
X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects