A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin.
Thulasi V, Veerapandiyan A, Pletcher BA, Tong CM, Ming X. A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin. Child Neurol Open. 2017 Jan-Dec; 4:2329048X17725610.