Author:
Tranel Elizabeth S.,McGowan Bridget,Drackley Andy,Epstein Leon G.,Rao Vamshi K.,Kuntz Nancy L.,Schwaede Abigail N.
Reference15 articles.
1. Brown-Vialetto-Van Laere syndrome: Clinical and neuroradiological findings of a genetically proven patient;Bandettini,2014
2. The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives;Bosch;Orphanet J. Rare Dis.,2012
3. Brown–Vialetto–van Laere and Fazio–Londe overlap syndromes: A clinical, biochemical and genetic study;Ciccolella;Neuromuscul. Disord.,2012
4. Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2;Foley;Brain, [online],2013
5. Brown-Vialetto-Van Laere syndrome, a Ponto-bulbar palsy with deafness, is caused by mutations in C20orf54;Green;Am. J. Hum. Genet.,2010