Novel mutation of the Spastin gene in familial spastic paraplegia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2001.590512.x/fullpdf
Reference9 articles.
1. Hereditary Spastic Paraplegia: advances in genetic research;The Hereditary Spastic Paraplegia Working Group;Neurology,1996
2. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2;Dürr;Brain,1996
3. Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p;Hazan;Hum Mol Genet,1994
4. Spastin, a novel AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia;Hazan;Nat Genet,1999
5. Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia;Fonknechten;Hum Mol Genet,2000
Cited by 9 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. Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males;Journal of the Neurological Sciences;2011-07
2. Chapter 17 Hereditary spastic paraparesis;Handbook of Clinical Neurology;2007
3. Clinical features of hereditary spastic paraplegia due to spastin mutation;Neurology;2006-07-10
4. Mutation Analysis of SPG4 and SPG3A Genes and Its Implication in Molecular Diagnosis of Korean Patients With Hereditary Spastic Paraplegia;Archives of Neurology;2005-07-01
5. Three Novel Mutations of the Spastin Gene in Chinese Patients With Hereditary Spastic Paraplegia;Archives of Neurology;2004-01-01
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