Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?

被引：21

作者：

Rabier, D

Diry, C

Rotig, A

Rustin, P

Heron, B

Bardet, J

Parvy, P

Ponsot, G

Marsac, C

Saudubray, JM

Munnich, A

Kamoun, P

机构：

[1] Hop Necker Enfants Malad, Lab Biochim Med B, F-75743 Paris 15, France

[2] Hop Necker Enfants Malad, Serv Malad Metab, F-75743 Paris, France

[3] Hop St Vincent de Paul, Serv Neurol, F-75674 Paris, France

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1998年 / 21卷 / 03期

关键词：

D O I：

10.1023/A:1005391300203

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：216 / 219

页数：4

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