A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia.

Source:http://linkedlifedata.com/resource/pubmed/id/7937987

Proc. Natl. Acad. Sci. U.S.A. 1994 Oct 25 91 22 10526-30

Download in:

View as

Triples

General Info

PMID
7937987