A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)-Reference-Cited by-同舟云学术

A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

Published:2002-11 Issue:5 Volume:71 Page:1189-1194
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Reid Evan,Kloos Mark,Ashley-Koch Allison,Hughes Lori,Bevan Simon,Svenson Ingrid K.,Graham Felicia Lennon,Gaskell Perry C.,Dearlove Andrew,Pericak-Vance Margaret A.,Rubinsztein David C.,Marchuk Douglas A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia;Ashley-Koch;Neurogenetics,2001

2. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics;Errico;Hum Mol Genet,2002

3. Hereditary spastic paraplegia: the pace quickens;Fink;Annals of Neurology,2002

4. Kinesin molecular motors: transport pathways, receptors, and human disease;Goldstein;Proc Natl Acad Sci USA,2001

5. Microtubule-based transport systems in neurons: the roles of kinesins and dynamins;Goldstein;Annu Rev Neurosci,2000

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