A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
In: Human Genetics 2021, 140(6):915–931. DOI: 10.1007/s00439-020-02254-z

Event
Veröffentlichung
(where)
Würzburg
(who)
Universität Würzburg
(when)
2022
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

DOI
10.1007/s00439-020-02254-z
URN
urn:nbn:de:bvb:20-opus-267740
Rights
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:30 AM CEST

Data provider

This object is provided by:
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
  • Universität Würzburg

Time of origin

  • 2022

Other Objects (12)