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Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: A new method to identify the G1528C mutation in genomic DNA showing its high frequency (≈90%) and identification of a new mutation (T2198C)
Author(s) -
Ijlst L.,
Ruiter J. P. N.,
Vreijling J.,
Wanders R. J. A.
Publication year - 1996
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/bf01799420
Subject(s) - university hospital , biochemistry , medicine , pediatrics