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Skin signs as early manifestations of Hutchinson-Gilford progeria syndrome
Archives of Diseases in Childhood, 06/26/2012

D’Erme AM et al. – Hutchinson–Gilford progeria syndrome (HGPS) is a rare, sporadic, autosomal dominant genetic disorder with phenotypic features of accelerated ageing due to a mutation of the lamin A (LMNA) gene.

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Skin signs as early manifestations of Hutchinson-Gilford progeria syndrome Archives of Diseases in Childhood, 06/26/2012

Skin signs as early manifestations of Hutchinson-Gilford progeria syndrome
Archives of Diseases in Childhood, 06/26/2012