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Results 1 - 6 of 6 for RIBOFLAVIN
  1. Riboflavin transporter deficiency neuronopathy 
    Riboflavin transporter deficiency neuronopathy is a disorder that affects nerve cells (neurons). Affected individuals typically have hearing loss caused by nerve ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  2. SLC52A3 gene 
    ... the C20orf54 gene) provides instructions for making a riboflavin transporter protein called RFVT3 (formerly known as RFT2). This protein moves (transports) a vitamin called riboflavin (also called vitamin B2) across the cell membrane. ...
    https://medlineplus.gov/genetics/gene/slc52a3 - Genetics
  3. SLC52A2 gene 
    The SLC52A2 gene provides instructions for making a riboflavin transporter protein called RFVT2 (formerly known as RFT3). This protein moves (transports) a vitamin called riboflavin (also called vitamin B2) across the cell membrane. ...
    https://medlineplus.gov/genetics/gene/slc52a2 - Genetics
  4. Glutaric acidemia type II 
    ... P, Gregersen N, Olsen RK. Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and ... AA. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. Brain. 2007 ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics
  5. ETFDH gene 
    ... AA. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. Brain. 2007 ...
    https://medlineplus.gov/genetics/gene/etfdh - Genetics
  6. ACAD9 deficiency 
    ... H, Rotig A, de Coo IF, Smeets HJ. Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics