Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.

Source:http://linkedlifedata.com/resource/pubmed/id/5648598

N. Engl. J. Med. 1968 Jun 13 278 24 1319-22

Download in:

View as

Triples

General Info

PMID
5648598