Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3-Reference-Cited by-同舟云学术

Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3

Published:2011 Issue:2 Volume:71 Page:106-112
ISSN:1423-0062
Container-title:Human Heredity
language:en
Short-container-title:Hum Hered

Author:

Ali Ghazanfar,Lee Kwanghyuk,Andrade Paula B.,Basit Sulman,Santos-Cortez Regie Lyn P.,Chen Leon,Jelani Musharraf,Ansar Muhammad,Ahmad Wasim,Leal Suzanne M.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss

2. A mutation in PDS causes non-syndromic recessive deafness

3. Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

4. A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

5. PedCheck: A Program for Identification of Genotype Incompatibilities in Linkage Analysis

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