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Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
Author(s) -
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.
Publication year - 1998
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1023/a:1005391300203
Subject(s) - library science , heron , genetics , biology , computer science , ecology