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

Stephan Klebe, Arnaud Lacour, Alexandra Durr, Tanya Stojkovic, Christel Depienne, Sylvie Forlani, Sandrine Poea-Guyon, Isabelle Vuillaume, Bernard Sablonniere, Patrick Vermersch, Alexis Brice, Giovanni Stevanin
Neurogenetics. 2007-01-05; 8(2): 155-157
DOI: 10.1007/s10048-006-0074-9


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1. Neurogenetics. 2007 Apr;8(2):155-7. Epub 2007 Jan 5.

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

Klebe S, Lacour A, Durr A, Stojkovic T, Depienne C, Forlani S, Poea-Guyon S,
Vuillaume I, Sablonniere B, Vermersch P, Brice A, Stevanin G.

DOI: 10.1007/s10048-006-0074-9
PMID: 17205300 [Indexed for MEDLINE]

Auteurs Bordeaux Neurocampus