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Article

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.

Neurogenetics - 1 Apr 2007

Klebe Stephan, Lacour Arnaud, Durr Alexandra, Stojkovic Tanya, Depienne Christel, Forlani Sylvie, Poea-Guyon Sandrine, Vuillaume Isabelle, Sablonniere Bernard, Vermersch Patrick, Brice Alexis, Stevanin Giovanni

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Source

Identifiers

PMID: 17205300
DOI: 10.1007/s10048-006-0074-9

Genes

NIPA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.PMID 17205300Read ↗

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Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3ASemantic proximity Read ↗

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