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SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia

C Paisan-Ruiz1, O Dogu, A Yilmaz

  • 1Molecular Genetics Unit, National Institute on Aging, National Institutes of Health, 35 Lincoln Drive, Building 35, Room 1A1015, Bethesda, MD 20824, USA. C.Paisan-Ruiz@ion.ucl.ac.uk

Neurology
|March 14, 2008
PubMed
Abstract

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