MC1R gene mutation and its association with oculocutaneous albinism type (OCA) phenotype in a consanguineous Pakistani family

✍ Scribed by Saleha, Shamim B.; Ajaml, Muhammad; Jamil, Muhammad; Nasir, Muhammad; Hameed, Abdul

• Book ID: 122896634
• Publisher: Elsevier Science
• Year: 2013
• Tongue: English
• Weight: 522 KB
• Volume: 70
• Category: Article
• ISSN: 0923-1811
• DOI: 10.1016/j.jdermsci.2012.11.591