Novel riboflavin transporter family RFVT/SLC52: Identification, nomenclature, functional characterization and genetic diseases of RFVT/SLC52

Molecular Aspects of Medicine

Volumn 34, Issue 2-3, 2013, Pages 693-701

  Yonezawa, Atsushi ^a   Inui, Ken Ichi ^a,b  

^a KYOTO UNIVERSITY   (Japan)

^b KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Brown Vialetto Van Laere (BVVL) syndrome; Multiple acyl CoA dehydrogenase deficiency (MADD); RFT; RFVT; Riboflavin; SLC52

Indexed keywords

CARRIER PROTEINS AND BINDING PROTEINS; FLAVINE ADENINE NUCLEOTIDE; FLAVINE MONONUCLEOTIDE; RIBOFLAVIN TRANSPORTER 1; RIBOFLAVIN TRANSPORTER 2; RIBOFLAVIN TRANSPORTER 3; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; AUTOSOMAL RECESSIVE DISORDER; BROWN VIALETTO VAN LAERE SYNDROME; ENZYME SPECIFICITY; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC DISORDER; HAPLOINSUFFICIENCY; HUMAN; MOLECULAR CLONING; MULTIPLE ACYL COA DEHYDROGENASE DEFICIENCY; NOMENCLATURE; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; REVIEW; SLC52A1 GENE; SLC52A2 GENE; SLC52A3 GENE; TISSUE DISTRIBUTION; TRANSPORT KINETICS;

ABSORPTION; BULBAR PALSY, PROGRESSIVE; CLONING, MOLECULAR; HEARING LOSS, SENSORINEURAL; HUMANS; MEMBRANE TRANSPORT PROTEINS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; MULTIPLE ACYL COENZYME A DEHYDROGENASE DEFICIENCY; PHENOTYPE; PHYLOGENY; POLYMORPHISM, GENETIC; RECEPTORS, G-PROTEIN-COUPLED; RIBOFLAVIN;

EID: 84875195134     PISSN: 00982997     EISSN: 18729452     Source Type: Journal    
DOI: 10.1016/j.mam.2012.07.014     Document Type: Review

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