A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency.

Source:http://linkedlifedata.com/resource/pubmed/id/11875054

Hum. Mol. Genet. 2002 Mar 1 11 5 599-604

Download in:

View as

Triples

General Info

PMID
11875054