TY  - GEN
AU  - Brassier,Anaïs
AU  - Ottolenghi,Chris
AU  - Boutron,Audrey
AU  - Bertrand,Anne-Marie
AU  - Valmary-Degano,Séverine
AU  - Cervoni,Jean-Paul
AU  - Chrétien,Dominique
AU  - Arnoux,Jean-Baptiste
AU  - Hubert,Laurence
AU  - Rabier,Daniel
AU  - Lacaille,Florence
AU  - de Keyzer,Yves
AU  - Di Martino,Vincent
AU  - de Lonlay,Pascale
TI  - Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome
SN  - 1096-7206
PY  - 2013///1112
KW  - Acidosis, Lactic
KW  - blood
KW  - Adult
KW  - Algeria
KW  - Child
KW  - Dihydrolipoamide Dehydrogenase
KW  - genetics
KW  - Female
KW  - Humans
KW  - Infant
KW  - Liver
KW  - pathology
KW  - Liver Failure, Acute
KW  - Male
KW  - Maple Syrup Urine Disease
KW  - Muscles
KW  - Mutation
KW  - Reye Syndrome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.ymgme.2013.01.017
ER  -