Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site

The MAG gene encodes myelin‐associated glycoprotein (MAG), an abundant protein involved in axon–glial interactions and myelination during nerve regeneration. Several members of a consanguineous family with a clinical syndrome reminiscent of Pelizaeus–Merzbacher disease and demyelinating leukodystrop...

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Detalles Bibliográficos
Autores principales: Roda, Ricardo H., FitzGibbon, Edmond J., Boucekkine, Houda, Schindler, Alice B., Blackstone, Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999596/
https://www.ncbi.nlm.nih.gov/pubmed/27606346
http://dx.doi.org/10.1002/acn3.329

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999596/
https://www.ncbi.nlm.nih.gov/pubmed/27606346
http://dx.doi.org/10.1002/acn3.329

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