Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment-Reference-Cited by-同舟云学术

Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment

Published:2007 Issue:7 Volume:28 Page:718-723
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Collin Rob W.J.,Kalay Ersan,Oostrik Jaap,Çaylan Refik,Wollnik Bernd,Arslan Selçuk,den Hollander Anneke I.,Birinci Yelda,Lichtner Peter,Strom Tim M.,Toraman Bayram,Hoefsloot Lies H.,Cremers Cor W.R.J.,Brunner Han G.,Cremers Frans P.M.,Karaguzel Ahmet,Kremer Hannie

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

2. , . 2000. Auditory brainstem response and electrocochleographic testing. In: , editors. The ear: comprehensive otology. Philadelphia: Lippincott Williams & Wilkins. p 231–241.

3. Nonsense-mediated mRNA decayin health and disease

4. Allegro, a new computer program for multipoint linkage analysis

5. easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data

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