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Autor:
Shagufta Shaikh, Nalini Bhat, Harshada Tawade, Jagannath Kurva, Susan Cherian, Suresh K. G. Shettigar, Anu Ghosh
Hearing loss is one of the most common sensory disorder and approximately 466 million people have disabling hearing loss worldwide. This study was conducted to identify the mutations in the GJB2, GJB3, and GJB6 genes in an Indian cohort with non-synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::496913e9131b16a1d5ff0384c1d8beb8