1. Genetic Studies of TYRP1 and SLC45A2 in Pakistani Patients with Nonsyndromic Oculocutaneous Albinism 
Tasleem Kausar, Thomas J. Jaworek, Nabeela Tariq, Sobia Sadia, Muhammad Ali, Rehan S. Shaikh, Zubair M. Ahmed 
Journal of Investigative Dermatology 
Volume 133, Issue 4, Pages (April 2013)
DOI: /jid
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2. Figure 1
Mutant alleles of TYRP1and SLC45A2 segregating in four Pakistani families. Pedigrees of four multigenerational Pakistani families cosegregating recessive nonsyndromic oculocutaneous albinism (OCA) and mutant alleles of TYRP1 or SLC45A2. The filled and clear symbols represent affected and unaffected individuals, respectively. The double lines indicate consanguineous marriages. TYRP1 or SLC45A2 mutations segregating in these families are also indicated. Photographs of multiple affected individuals from each family are also shown. The numbers on the family pedigrees indicate individuals shown. All the individuals have given written consent to show their images. For several of the affected individuals, multiple photographs taken at different ages revealed no significant changes in the pigmentation of the hair, iris, or skin. Some of the affected individuals have used hair dyes.
Journal of Investigative Dermatology  , DOI: ( /jid )
Copyright © 2013 The Society for Investigative Dermatology, Inc Terms and Conditions