Genetic Analysis of Oculocutaneous Albinism Type1A (OCA1A) in an Iranian Family
"nBackground: Oculocutaneous albinism type1 (OCA1) is characterized by the absence of melanin pigmentation. The muta­tion on TYR gene makes OCA1 as an autosomal recessive genetic disorder. In this study, we delineated the genetic analysis of an Iranian family with four members affected...
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| Main Authors: | , , |
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| Format: | Book |
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Tehran University of Medical Sciences,
2010-03-01T00:00:00Z.
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