Title |
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans |
|---|---|
Involved |
Barbara Vona (Verfasser)
Neda Mazaheri (Verfasser) Sheng-Jia Lin (Verfasser) Lucy A. Dunbar (Verfasser)
Reza Maroofian (Verfasser)
Hela Azaiez (Verfasser) Kevin T. Booth (Verfasser) Sandrine Vitry (Verfasser) Aboulfazl Rad (Verfasser) Franz Rüschendorf (Verfasser) Pratishtha Varshney (Verfasser) Ben Fowler (Verfasser) Christian Beetz (Verfasser) Kumar N. Alagramam (Verfasser) David Murphy (Verfasser) Gholamreza Shariati (Verfasser) Alireza Sedaghat (Verfasser) Henry Houlden (Verfasser) Cassidy Petree (Verfasser) Shruthi VijayKumar (Verfasser) Richard J. H. Smith (Verfasser) Thomas Haaf (Verfasser) Aziz El-Amraoui (Verfasser) Michael R. Bowl (Verfasser) Gaurav K. Varshney (Verfasser) Hamid Galehdari (Verfasser) SpringerLink (Online service) (Sonstige) |
Published in |
Human genetics 26.1.2021, Seite 1-17 |
Published |
2021 |
Language |
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Country |
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Topic |
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Subject |
Human Genetics. |
DDC notation |
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Persistent identifier |
urn:nbn:de:101:1-2021031718125959671468 (URN) |
Record ID |
1229568859 |
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