Article

Identification of Known and Novel Genetic Variants in Sensorineural Hearing Loss: Insights from Whole Exome Sequencing in Indian Families

2025-07-01

Abstract excerpt

<title>Abstract</title> <p>Background Hearing loss is one of the most common congenital anomalies and is a complex etiologically diverse condition. Molecular genetic characterization of hearing loss remains challenging owing to the high genetic heterogeneity. This study aimed to screen for potential disease-causing genetic variations in a specific cohort of Indian patients with congenital bilateral severe-to-pro...

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Literature Corpus work: e1ee2b7e-8b0b-53e0-8b95-53f3d24a2d5d
DOI: 10.21203/rs.3.rs-6930320/v1

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