PERSISTENT HYPOCITRULLINAEMIA AS A MARKER FOR MTDNA NARP T-8993 G-MUTATION

Citation
D. Rabier et al., PERSISTENT HYPOCITRULLINAEMIA AS A MARKER FOR MTDNA NARP T-8993 G-MUTATION, Journal of inherited metabolic disease, 21(3), 1998, pp. 216-219
Citations number
6
Categorie Soggetti
Endocrynology & Metabolism","Genetics & Heredity
ISSN journal
01418955
Volume
21
Issue
3
Year of publication
1998
Pages
216 - 219
Database
ISI
SICI code
0141-8955(1998)21:3<216:PHAAMF>2.0.ZU;2-X