The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations

Deafness encompasses a series of etiologically heterogeneous disorders with mutations in more than 400 independent genes. However, several studies indicate that a large proportion of both syndromic and nonsyndromic forms of deafness in the racially diverse Indian and Pakistani populations are caused...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Genet Test Mol Biomarkers
Egile Nagusiak: Yan, Denise, Kannan-Sundhari, Abhiraami, Vishwanath, Subramanian, Qing, Jie, Mittal, Rahul, Kameswaran, Mohan, Liu, Xue Zhong
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Mary Ann Liebert, Inc. 2015
Gaiak:
Original Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4575533/
https://ncbi.nlm.nih.gov/pubmed/26186295
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2015.0023
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