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Riboflavin Transporter Deficiency or Brown-Vialetto-Van Laere Syndrome

Enrico Bertini   +2 more
openaire   +1 more source

Longitudinal riboflavin response in homozygous SLC52A2 p.Pro134Leu: a Turkish kindred with riboflavin transporter deficiency type 2

Neuromuscular Disorders
Ali Zeki Bedir, Haluk Topaloğlu
openaire   +1 more source
riboflavin
brown-vialetto-van laere syndrome
neurodegenerative disease
vitamin b2
energy metabolism
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