Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome
Open Access
- 3 April 2008
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 82 (4), 992-1002
- https://doi.org/10.1016/j.ajhg.2008.03.004
Abstract
No abstract availableKeywords
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