Severe axonal neuropathy is a late manifestation of SPG11

Complex hereditary spastic paraplegia (HSP) is a clinically heterogeneous group of disorders usually inherited in an autosomal recessive manner. In the past, complex recessive spastic paraplegias have been frequently associated with SPG11 mutations but also with defects in SPG15, SPG7 and a handful...

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Detalles Bibliográficos
Autores principales: Manole, Andreea, Chelban, Viorica, Haridy, Nourelhoda A., Hamed, Sherifa A., Berardo, Andrés, Reilly, Mary M., Houlden, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065903/
https://www.ncbi.nlm.nih.gov/pubmed/27544499
http://dx.doi.org/10.1007/s00415-016-8254-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065903/
https://www.ncbi.nlm.nih.gov/pubmed/27544499
http://dx.doi.org/10.1007/s00415-016-8254-5

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