B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker–Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss

Title
B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker–Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss
Authors
Keywords
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Journal
NEUROPEDIATRICS
Volume 49, Issue 04, Pages 289-295
Publisher
Georg Thieme Verlag KG
Online
2018-05-24
DOI
10.1055/s-0038-1651519

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