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l-2-Hydroxyglutaric aciduria: Clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variability

✍ Scribed by A. Larnaout; R. Amouri; M. Kefi; F. Hentati


Publisher
Springer
Year
2008
Tongue
English
Weight
241 KB
Volume
31
Category
Article
ISSN
0141-8955

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