Mutational Analysis of Oculocutaneous Albinism: A Compact Review

Article, Review English OPEN
Kamaraj, Balu; Purohit, Rituraj;
(2014)

Oculocutaneous albinism (OCA) is an autosomal recessive disorder caused by either complete lack of or a reduction of melanin biosynthesis in the melanocytes. The OCA1A is the most severe type with a complete lack of melanin production throughout life, while the milder f... View more
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