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Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C 6 –C 14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?
Author(s) -
PollThe B. T.,
Bonnefont J. P.,
Ogier H.,
Charpentier C.,
Pelet A.,
Le Fur J. M.,
Jakobs C.,
Kok R. M.,
Duran M.,
Divry P.,
Scotto J.,
Saudubray J. M.
Publication year - 1988
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 - 10.1007/bf01804230
Subject(s) - medicine , pediatrics