DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Mishra S, Pandey H, Srivastava P, Mandal K, Phadke SR.
Connexin 26 (GJB2) mutations associated with non-syndromic hearing loss (NSHL).
Indian J Pediatr 2018;
85 (12) 1061-1066
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