Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.

Source:http://linkedlifedata.com/resource/pubmed/id/1496017

Proc. Natl. Acad. Sci. U.S.A. 1992 Aug 1 89 15 7232-6

Download in:

View as

Triples

General Info

PMID
1496017