A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism.

Source:http://linkedlifedata.com/resource/pubmed/id/1711223

Proc. Natl. Acad. Sci. U.S.A. 1991 Jun 15 88 12 5272-6

Download in:

View as

Triples

General Info

PMID
1711223