Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia.
Depienne C; Fedirko E; Forlani S; Cazeneuve C; Ribaï P; Feki I; Tallaksen C; Nguyen K; Stankoff B; Ruberg M; Stevanin G; Durr A; Brice A; Journal Of Medical Genetics, 2007, vol. 44, issue 4, p 281, ISSN 14686244. ISBN 14686244.

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