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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
Al Dhaibani, Muna, El-Hattab, Ayman, Ismayl, Omar, Suleiman, JehanLanguage:
english
Journal:
Neuropediatrics
DOI:
10.1055/s-0038-1651519
Date:
May, 2018
File:
PDF, 407 KB
english, 2018