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A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)

✍ Scribed by S. Kamran-ul-Hassan Naqvi; S.I. Raza; A.K. Naveed; P. John; W. Ahmad

No coin nor oath required. For personal study only.

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