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A whole-exome analysis of non-syndromic hearing loss patients from India reveals a wide spectrum of known and novel mutations

2023-02-10

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<title>Abstract</title> <p>Background Non-syndromic hearing loss (NSHL) is characterized by congenital mild-to-profound sensorineural hearing impairment. It affects 1 in 1000 neonates in India. While we have a large genetically deaf population in India, our knowledge about the specific causes behind the disorder is almost non-existent. We carried out clinical audiological characterization in a cohort of 43 NSHL...

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Literature Corpus work
a7b84b85-cb14-5dfb-9dc6-40a38dab9187
DOI
10.21203/rs.3.rs-2549071/v1
Open publication

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