Mutations in CDC14A , Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness-Reference-Cited by-同舟云学术

Mutations in CDC14A , Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness

Published:2016-06 Issue:6 Volume:98 Page:1266-1270
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Delmaghani Sedigheh,Aghaie Asadollah,Bouyacoub Yosra,El Hachmi Hala,Bonnet Crystel,Riahi Zied,Chardenoux Sebastien,Perfettini Isabelle,Hardelin Jean-Pierre,Houmeida Ahmed,Herbomel Philippe,Petit Christine

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. Hereditary hearing loss: From human mutation to mechanism;Lenz;Hear. Res.,2011

2. Auditory brainstem response and electrocochleographic testing;Dirks,2000

3. Otoacoustic emissions, their origin in cochlear function, and use;Kemp;Br. Med. Bull.,2002

4. The phosphatase Cdc14 triggers mitotic exit by reversal of Cdk-dependent phosphorylation;Visintin;Mol. Cell,1998

5. Cell cycle: new functions for Cdc14 family phosphatases;Trautmann;Curr. Biol.,2002

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