Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!

Homozygous mutations in MAG, encoding the myelin‐associated glycoprotein, a transmembrane component of the myelin sheath, have been associated with SPG 75 recessive spastic paraplegia. Here, we report the first patient with two compound heterozygous novel MAG mutations (p.A151V and p.S373R) and earl...

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Detalles Bibliográficos
Autores principales: Roubertie, Agathe, Charif, Majida, Meyer, Pierre, Manes, Gael, Meunier, Isabelle, Taieb, Guillaume, Junta Morales, Raul, Guichet, Agnès, Delettre, Cecile, Sarzi, Emmanuelle, Leboucq, Nicolas, Rivier, François, Lenaers, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689693/
https://www.ncbi.nlm.nih.gov/pubmed/31402626
http://dx.doi.org/10.1002/acn3.50860

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689693/
https://www.ncbi.nlm.nih.gov/pubmed/31402626
http://dx.doi.org/10.1002/acn3.50860

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