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Updated: Sep 23, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights

Zafar Ali1, Najeeb Ullah1, Muneeba Bibi2

  • 1Centre for Biotechnology and Microbiology, University of Swat, Charbagh, Swat, Khyber Pakhtunkhwa, Pakistan.

Annals of Human Genetics
|September 22, 2026
PubMed
Abstract

Keywords:
3D structuresESRP1MSRB3TMC1exome sequencinghearing lossmissense variant

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