SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature

    Anuradha Bishnoi, Aarushi Arunima, Keshavamurthy Vinay, Muthu Sendhil Kumaran, Davinder Parsad
    Studysummary This literature review reports that mutations in the SASH1 gene are linked to different pigmentation disorders, including dyschromatosis universalis hereditaria and lentiginosis. It further suggests SASH1's significant role in melanocyte processes and its potential as a target for developing treatments for these conditions.
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