Riboflavin in Brown-Vialetto-Van Laere Syndrome
Investigators at Great Ormond Street Hospital, London, UK, and multiple centers internationally report the response to high-dose oral riboflavin therapy in 18 patients from 13 families with mutations in SLC5ZA2, encoding riboflavin transporter RTVT2, a new causative gene for Brown-Vialetto-Van Laere...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Pediatric Neurology Briefs Publishers
2014-03-01
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| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/189 |
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