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SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype.
- Source :
-
Revue neurologique [Rev Neurol (Paris)] 2019 Oct; Vol. 175 (9), pp. 572-574. Date of Electronic Publication: 2019 May 27. - Publication Year :
- 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 genetics
Spastic Paraplegia, Hereditary pathology
Urinary Incontinence complications
Urinary Incontinence diagnosis
Urinary Incontinence genetics
Spastic Paraplegia, Hereditary diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 0035-3787
- Volume :
- 175
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Revue neurologique
- Publication Type :
- Report
- Accession number :
- 31147273
- Full Text :
- https://doi.org/10.1016/j.neurol.2019.01.397