Publication

Giebel LB, Strunk KM, King RA, Hanifin JM, Spritz RA, A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism. Proc Natl Acad Sci U S A87:3255-8 1990
PubMed ID: 1970634

Records Return:  (1) Show
 
Catalog IDGenderDescription
GM11345FemaleALBINISM, OCULOCUTANEOUS, TYPE 1A; OCA1A