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Early signs and course of disease of glutaryl‐CoA dehydrogenase deficiency
Author(s) -
Hoffmann G. F.,
Böhles H. J.,
Burlina A.,
Duran M.,
Herwig J.,
Lehnert W.,
Leonard J. V.,
Muntau A.,
PleckoStarting F. K.,
SupertiFurga A.,
Trefz F. K.,
Christensen E.
Publication year - 1995
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/bf00711759
Subject(s) - medicine , pediatrics , emergency department , university hospital , library science , family medicine , psychiatry , computer science