| Literature DB >> 15452312 |
M Fichera1, M Lo Giudice, M Falco, M Sturnio, S Amata, O Calabrese, S Bigoni, E Calzolari, M Neri.
Abstract
Hereditary spastic paraplegias (HSPs) are characterized by progressive lower extremity spasticity due to an axonal degeneration of motor and sensory neurons. We report a four-generation pedigree segregating an autosomal dominant phenotype for HSP and showing a linkage to the SPG10 locus, coding for Kinesin family member 5A. Subsequent to a denaturing high performance liquid chromatography (dHPLC) mutation screening we found a new missense mutation 838C>T (R280C) at an invariant arginine residue in a region involved in the microtubule binding activity.Entities:
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Year: 2004 PMID: 15452312 DOI: 10.1212/01.wnl.0000138731.60693.d2
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910