Links
[1] http://omim.org/entry/607882
[2] https://disorders.eyes.arizona.edu/references/slc52a2-mutations-cause-scabd2-phenotype-second-report
[3] https://disorders.eyes.arizona.edu/references/treatable-childhood-neuronopathy-caused-mutations-riboflavin-transporter-rfvt2
[4] https://disorders.eyes.arizona.edu/references/exome-sequencing-reveals-riboflavin-transporter-mutations-cause-motor-neuron-disease
[5] https://disorders.eyes.arizona.edu/references/brown-vialetto-van-laere-syndrome-large-inbred-lebanese-family-confirmation-autosomal