Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome.

Source:http://linkedlifedata.com/resource/pubmed/id/9674913

Am. J. Med. Genet. 1998 Jun 30 78 2 179-81

Download in:

View as

Triples

General Info

PMID
9674913