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A novel ACAD8 mutation in asymptomatic patients with isobutyryl‐ CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum
Author(s) -
Yun J.W.,
Jo K.I.,
Woo H.I.,
Lee S.Y.,
Ki C.S.,
Kim J.W.,
Song J.,
Lee D.H.,
Lee Y.W.,
Park H.D.
Publication year - 2015
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12350
Subject(s) - medicine , asymptomatic , family medicine
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