Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia.
Depienne, Christel; Fedirko, Estelle; Forlani, Sylvie; Cazeneuve, Cécile; Ribaï, Pascale; Feki, Imed; Tallaksen, Chantal; Nguyen, Karine; Stankoff, Bruno; Ruberg, Merle; Stevanin, Giovanni; Durr, Alexandra; Brice, Alexis; Journal of Medical Genetics, 2007, vol. 44, issue 4, p 281, ISSN 00222593. ISBN 14686244.

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