A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options
Author:
Affiliation:
1. Department of Human Genetics and Molecular Medicine, School of Health Sciences Central University of Punjab Bathinda India
2. Department of Pediatrics Medicine Post Graduate Institute of Medical Education and Research Chandigarh India
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14228
Reference278 articles.
1. Genetics of Nonsyndromic Congenital Hearing Loss
2. Human Nonsyndromic Sensorineural Deafness
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