Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
作者信息
Rabier D, Diry C, Rotig A, Rustin P, Heron B, Bardet J, Parvy P, Ponsot G, Marsac C, Saudubray J M, Munnich A, Kamoun P
机构信息
Laboratoire Biochimie B, Hôpital Necker-Enfants Malades, Paris, France.
出版信息
J Inherit Metab Dis. 1998 Jun;21(3):216-9. doi: 10.1023/a:1005391300203.
PMID:9686360
Abstract
摘要
Zotero 插件