Author:
Manga Prashiela,Kromberg Jennifer G.R.,Turner Angela,Jenkins Trefor,Ramsay Michele
Subject
Genetics(clinical),Genetics
Reference20 articles.
1. Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as “OCA3”;Boissy;Am J Hum Genet,1996
2. Dinucleotide repeat polymorphism at the human TYRP1 locus;Box;Hum Mol Genet,1994
3. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism;Durham-Pierre;Nat Genet,1994
4. The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids;Kedda;Am J Hum Genet,1994
5. Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa;Kerr;Hum Mutat,2000
Cited by
29 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献