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Riboflavin Transporter 1 Deficiency Caused by a Homozygous Single Exonal Deletion of SLC52A1
Urim Kang, Da Hae Yang, Sang Ook Nam, Yun-jin Lee, Gyu Min Yeon
Ann Child Neurol. 2020;28(4):160-163. Published online 2020 Sep 4 DOI: https://doi.org/10.26815/acn.2020.00136
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Citations to this article as recorded by
 Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum
Sarah C. Grünert, Athanasia Ziagaki, André Heinen, Anke Schumann, Sara Tucci, Ute Spiekerkoetter, Miriam Schmidts
Genes.2023; 14(7): 1408. CrossRef
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