Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome
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| Description | scientific article |
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author: Chokri Mhiri Nizar Elleuch Filippo Maria Santorelli Alexandra Durr Sylvie Forlani Giovanni Stevanin Abdelmadjid Hamri Amir Boukhris Elodie Martin Alexis Brice Alexander Lossos Imed Feki Michael Hutchinson Paola S Denora Sylvain Hanein Cyril Goizet |
| Publication date | April 1, 2008 |
| Language | English |
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