Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.

Article Details

Citation
Copy to clipboard

Spritz RA, Strunk KM, Giebel LB, King RA

Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.

N Engl J Med. 1990 Jun 14;322(24):1724-8.

PubMed ID
2342539 [ View in PubMed
]
Abstract

Not Available

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
TyrosinaseP14679Details