High frequency ofOTOFmutations in Chinese infants with congenital auditory neuropathy spectrum disorder-Reference-Cited by-同舟云学术

High frequency ofOTOFmutations in Chinese infants with congenital auditory neuropathy spectrum disorder

Published:2016-03-11 Issue:3 Volume:90 Page:238-246
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Zhang Q.-J.¹,Han B.¹,Lan L.¹,Zong L.¹,Shi W.¹,Wang H.-Y.¹,Xie L.-Y.¹,Wang H.¹,Zhao C.¹,Zhang C.¹,Yin Z.-F.¹,Wang D.-Y.¹,Petit C.²,Guan J.¹,Wang Q.-J.¹

Affiliation:

1. Department of Otolaryngology/ Head and Neck Surgery, Chinese PLA Institute of Otolaryngology; Chinese PLA General Hospital; Beijing China

2. Unité de Génétique et Physiologie de l'Audition; Institut Pasteur, Collège de France; Paris France

Funder

National Key Basic Research Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference25 articles.

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2. The varieties of auditory neuropathy;Starr;J Basic Clin Physiol Pharmacol,2000

3. Identification of auditory neuropathy in infants and children;Sininger;Seminars in 525 Hearing,2002

4. Auditory neuropathy spectrum disorder: a review;Norrix;J Speech Lang Hear Res,2014

5. The genetic basis of auditory neuropathy spectrum disorder (ANSD);Manchaiah;Int J Pediatr Otorhinolaryngol,2011

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