Premium
Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency
Author(s) -
Przyrembel H.,
Jakobs C.,
Ijlst L.,
Klerk J. B. C.,
Wanders R. J. A.
Publication year - 1991
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/bf01799932
Subject(s) - dehydrogenase , human genetics , endocrinology , metabolic disease , medicine , enzyme , biochemistry , chemistry , gene
Summary A new case of 3‐hydroxyacyl‐CoA dehydrogenase deficiency is described with a relatively benign course.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom