Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia-Reference-Cited by-同舟云学术

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Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia

Published:2001-01-30 Issue:2 Volume:3 Page:91-97
ISSN:1364-6745
Container-title:Neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Ashley-Koch Allison,Bonner Erin R.,Gaskell P. Craig,West Sandra G.,Tim Richard,Wolpert Chantelle M.,Jones Rodney,Farrell Carolyn D.,Nance Martha,Svenson Ingrid K.,Marchuk Douglas A.,Boustany Rose-Mary N.,Vance Jeffery M.,Scott William K.,Pericak-Vance Margaret A.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s100480000098.pdf

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12;Journal of Clinical Investigation;2012-02-01

2. Clinical and genetic findings in a series of Italian children with pure hereditary spastic paraplegia;European Journal of Neurology;2010-12-15

3. Molecular Genetics of Hereditary Spastic Paraplegias;eLS;2009-09-15

4. Chapter 17 Hereditary spastic paraparesis;Handbook of Clinical Neurology;2007

5. Chapter 15 Autosomal Dominant Spastic Paraplegia: Loci/Genes Other Than SPG4 (spastin);Spinocerebellar Degenerations: The Ataxias and Spastic Paraplegias;2007

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