- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1432-1203
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans ; day:26 ; month:1 ; year:2021 ; pages:1-17
Human genetics; (26.1.2021), 1-17
- Creator
-
Vona, Barbara
Mazaheri, Neda
Lin, Sheng-Jia
Dunbar, Lucy A.
Maroofian, Reza
Azaiez, Hela
Booth, Kevin T.
Vitry, Sandrine
Rad, Aboulfazl
Rüschendorf, Franz
Varshney, Pratishtha
Fowler, Ben
Beetz, Christian
Alagramam, Kumar N.
Murphy, David
Shariati, Gholamreza
Sedaghat, Alireza
Houlden, Henry
Petree, Cassidy
VijayKumar, Shruthi
Smith, Richard J. H.
Haaf, Thomas
El-Amraoui, Aziz
Bowl, Michael R.
Varshney, Gaurav K.
Galehdari, Hamid
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s00439-020-02254-z
- URN
-
urn:nbn:de:101:1-2021031718125959671468
- 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
- Vona, Barbara
- Mazaheri, Neda
- Lin, Sheng-Jia
- Dunbar, Lucy A.
- Maroofian, Reza
- Azaiez, Hela
- Booth, Kevin T.
- Vitry, Sandrine
- Rad, Aboulfazl
- Rüschendorf, Franz
- Varshney, Pratishtha
- Fowler, Ben
- Beetz, Christian
- Alagramam, Kumar N.
- Murphy, David
- Shariati, Gholamreza
- Sedaghat, Alireza
- Houlden, Henry
- Petree, Cassidy
- VijayKumar, Shruthi
- Smith, Richard J. H.
- Haaf, Thomas
- El-Amraoui, Aziz
- Bowl, Michael R.
- Varshney, Gaurav K.
- Galehdari, Hamid
- SpringerLink (Online service)
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Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria