SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage

SPG11 mutations are the major cause of autosomal recessive Hereditary Spastic Paraplegia. The disease has a wide phenotypic variability indicating many regions of the nervous system besides the corticospinal tract are affected. Despite this, anatomical and phenotypic characterization is restricted....

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Bibliographic Details
Published in:Neuroimage Clin
Main Authors: Faber, Ingrid, Martinez, Alberto Rolim Muro, de Rezende, Thiago Junqueira Ribeiro, Martins, Carlos Roberto, Martins, Melina Pazian, Lourenço, Charles Marques, Marques, Wilson, Montecchiani, Celeste, Orlacchio, Antonio, Pedroso, Jose Luiz, Barsottini, Orlando Graziani Povoas, Lopes-Cendes, Íscia, França, Marcondes Cavalcante
Format: Artigo
Language:Inglês
Published: Elsevier 2018
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Regular Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6008284/
https://ncbi.nlm.nih.gov/pubmed/29946510
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2018.05.031
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