A Rare Syndrome of GRID2 Deletion in 2 Siblings

por Veerapandiyan, Aravindhan, Enner, Stephanie, Thulasi, Venkatraman, Ming, Xue
Publicado 2017

A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin

por Thulasi, Venkatraman, Veerapandiyan, Aravindhan, Pletcher, Beth A., Tong, Chun M., Ming, Xue
Publicado 2017