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SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype
- Source :
- Revue Neurologique. 175:572-574
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
- Subjects :
- Pathology
medicine.medical_specialty
medicine.diagnostic_test
business.industry
Hereditary spastic paraplegia
Magnetic resonance imaging
Neurologic diagnosis
medicine.disease
Phenotype
Chronic disease
Neurology
Mutation (genetic algorithm)
medicine
Missense mutation
Gait disorders
Neurology (clinical)
business
Subjects
Details
- ISSN :
- 00353787
- Volume :
- 175
- Database :
- OpenAIRE
- Journal :
- Revue Neurologique
- Accession number :
- edsair.doi...........74816981d059c3319b877b9e32adbbce
- Full Text :
- https://doi.org/10.1016/j.neurol.2019.01.397