Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.
作者信息
Rosenberg L E, Lilljeqvist A C, Hsia Y E
出版信息
N Engl J Med. 1968 Jun 13;278(24):1319-22. doi: 10.1056/NEJM196806132782404.
PMID:5648598
Abstract
摘要
Zotero 插件