Open AccessMitochondrial Genome Screening Identified 26 Novel Variants in Children with Nonsyndromic Congenital Hearing Impairment
Author(s) -
Hema Bindu L,
Shehnaz Sultana,
P.P. Reddy
Publication year - 2022
Publication title -
archives of internal medicine research
Language(s) - English
Resource type - Journals
ISSN - 2688-5654
DOI - 10.26502/aimr.0095
Subject(s) - mitochondrial dna , genetics , gene , biology , hearing loss , transfer rna , genome , medicine , rna , audiology
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