Article

Identification of MITF Gene Mutation in Porcupines: A Novel Link to Congenital Deafness and Pigmentation Disorders

2024-08-26

Abstract excerpt

<title>Abstract</title> <p>Worldwide, congenital deafness and pigmentation disorders impact millions with their diverse manifestations, and among these genetic conditions, mutations in the Microphthalmia-associated transcription factor (<italic>MITF</italic>: OMIM#156845) gene are notable for their profound effects on melanocyte development and auditory functions. We first discovered congenital deafness in mutant...

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Literature Corpus work: 950e8897-df6c-5bc6-9708-ae572170fdf9
DOI: 10.21203/rs.3.rs-4679701/v1

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