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Article

CAPN1 mutations are associated with a syndrome of combined spasticity and ataxia.

Journal of neurology - 1 May 2017

Tadic Vera, Klein Christine, Hinrichs Frauke, Münchau Alexander, Lohmann Katja, Brüggemann Norbert

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Identifiers

PMID: 28321562
DOI: 10.1007/s00415-017-8464-5

Genes

CAPN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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CAPN1 mutations are associated with a syndrome of combined spasticity and ataxia.PMID 28321562Read ↗

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Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review.Semantic proximity Read ↗

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia.Semantic proximity Read ↗

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.Semantic proximity Read ↗

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