A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)-Reference-Cited by-同舟云学术

A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)

Published:2008-12 Issue:6 Volume:83 Page:752-759
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lin Pengfei,Li Jianwei,Liu Qiji,Mao Fei,Li Jisheng,Qiu Rongfang,Hu Huili,Song Yang,Yang Yang,Gao Guimin,Yan Chuanzhu,Yang Wanling,Shao Changshun,Gong Yaoqin

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference17 articles.

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3. Hereditary spastic paraplegia;Fink;Curr. Neurol. Neurosci. Rep.,2006

4. Advances in the hereditary spastic paraplegias;Fink;Exp. Neurol.,2003

5. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia;Hazan;Nat. Genet.,1999

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