Everything, everywhere: FSHD as a model for complex genetic disease.

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Europe PMCPublished 2026Genetics & Molecular BiologyMolecular & Cellular Biology
Journal
Trends in genetics : TIG
Record source
Europe PMC Research Library

Abstract / Description

Medical genetics can reveal how genetic variations shape human biology by addressing a critical question: how does a genetic lesion become a phenotype? Facioscapulohumeral muscular dystrophy (FSHD), exemplifies how a seemingly simple genetic lesion can affect multiple layers of cellular regulation, affecting 'everything, everywhere all at once'.
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