SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype

SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype

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Bibliographic Details
Published in:Revue neurologique Vol. 175; no. 9; pp. 572 - 574
Main Authors: Souza, P.V.S., Silva, L.H.L., Badia, B.M.L., Farias, I.B., Pinto, W.B.V.R., Oliveira, A.S.B.
Format: Journal Article
Language:English
Published: France Elsevier Masson SAS 01-10-2019
Subjects:
Brazil
Calpain - genetics
Chronic Disease
Depression - complications
Depression - diagnosis
Depression - genetics
Female
Gait Disorders, Neurologic - diagnosis
Gait Disorders, Neurologic - etiology
Humans
Magnetic Resonance Imaging
Middle Aged
Mutation, Missense
Phenotype
Spastic Paraplegia, Hereditary - diagnosis
Spastic Paraplegia, Hereditary - genetics
Spastic Paraplegia, Hereditary - pathology
Urinary Incontinence - complications
Urinary Incontinence - diagnosis
Urinary Incontinence - genetics
Brazil
HSP
FTD
Online Access:Get full text
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Description
ISSN:0035-3787
DOI:10.1016/j.neurol.2019.01.397