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 a...
Main Authors: | H Pour-Jafari, A Zamanian, B Pour-Jafari |
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Format: | Article |
Language: | English |
Published: |
Tehran University of Medical Sciences
2010-03-01
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Series: | Iranian Journal of Public Health |
Subjects: | |
Online Access: | http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/15198.pdf&manuscript_id=15198 |
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