Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with
ATPases Associated with Diverse Cellular Activities
/ genetics
Adult
Cerebellar Ataxia
/ genetics
Cohort Studies
Electromyography
Female
Humans
Loss of Function Mutation
Magnetic Resonance Imaging
Male
Metalloendopeptidases
/ genetics
Middle Aged
Paraplegia
/ genetics
Phenotype
Polymorphism, Single Nucleotide
Spastic Paraplegia, Hereditary
/ genetics
White People
/ genetics
Young Adult
Journal
Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060
Informations de publication
Date de publication:
04 06 2019
04 06 2019
Historique:
received:
14
10
2018
accepted:
31
01
2019
pubmed:
10
5
2019
medline:
24
12
2019
entrez:
10
5
2019
Statut:
ppublish
Résumé
We took advantage of a large multinational recruitment to delineate genotype-phenotype correlations in a large, trans-European multicenter cohort of patients with spastic paraplegia gene 7 ( We analyzed clinical and genetic data from 241 patients with Patients with This is the largest
Identifiants
pubmed: 31068484
pii: WNL.0000000000007606
doi: 10.1212/WNL.0000000000007606
pmc: PMC6556095
doi:
Substances chimiques
Metalloendopeptidases
EC 3.4.24.-
SPG7 protein, human
EC 3.4.24.-
ATPases Associated with Diverse Cellular Activities
EC 3.6.4.-
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2679-e2690Informations de copyright
© 2019 American Academy of Neurology.
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