학술논문
P.367 - A case of childhood onset of treatable sensory neuronopathy caused by mutations in riboflavin transporter RFVT2 presenting as pure sensory ataxia with excellent response to riboflavin – a five year follow up
Document Type
Abstract
Source
In Neuromuscular Disorders October 2017 27 Supplement 2:S206-S206
Subject
Language
ISSN
0960-8966