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Brown‐Vialetto‐Van Laere and Fazio Londe syndromes: defects of riboflavin transport with biochemical similarities to multiple acyl‐CoA dehydrogenation defects (MADD)
Author(s) -
Bennett Michael J.
Publication year - 2012
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/s10545-012-9519-5
Subject(s) - riboflavin , flavin group , flavin mononucleotide , flavin adenine dinucleotide , flavoprotein , biochemistry , genetics , cofactor , chemistry , biology , enzyme