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Passmore et al., 1999 - Google Patents

Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population

Passmore et al., 1999

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Document ID
4059660741215280602
Author
Passmore L
Kaesmann-Kellner B
Weber B
Publication year
Publication venue
Human genetics

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Albinism is a heterogeneous group of genetic disorders resulting from deficiencies in pigmentation. Clinically, it is divided into ocular (OA) and oculocutaneous albinism (OCA). OCA involves lack of pigment in the skin, hair, and eyes and results from mutations in the …
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