Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 10(42), p. 1321-1335, 2021
DOI: 10.1002/humu.24260
Links
Tools
Variants of human CLDN9 cause mild to profound hearing loss
Journal article published in 2021 by
Memoona Ramzan 
,
Oumaima Zarrik ,
Christophe Philippe ,
Cristina Fenollar‐Ferrer ,
Inna A. Belyantseva ,
Yoko Nakano ,
Risa Tona ,
Zunaira Munir ,
Rizwan Yousaf ,
Hafiza Idrees ,
Midhat Salman ,
Rasheeda Basheer ,
Sophie Nambot ,
Antonio Vitobello ,
Ayesha Imtiaz
and other authors.
,
Oumaima Zarrik ,
Christophe Philippe ,
Cristina Fenollar‐Ferrer ,
Inna A. Belyantseva ,
Yoko Nakano ,
Risa Tona ,
Zunaira Munir ,
Rizwan Yousaf ,
Hafiza Idrees ,
Midhat Salman ,
Rasheeda Basheer ,
Sophie Nambot ,
Antonio Vitobello ,
Ayesha Imtiaz
and other authors.
This paper is made freely available by the publisher.
Full text: Download
Published version:
archiving forbidden
Data provided by 