Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25-Reference-Cited by-同舟云学术

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

Published:2008-07 Issue:3 Volume:9 Page:
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Macedo-Souza Lúcia Inês,Kok Fernando,Santos Silvana,Licinio Luciana,Lezirovitz Karina,Nascimento Rafaella M. P.,Bueno Clarissa,Martyn Marcília,Leão Emília K. E. A.,Zatz Mayana

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-008-0130-8.pdf

Reference6 articles.

1. Zatz M, Penha-Serrano C, Otto PA (1976) X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg. J Med Genet 13:217–222

2. Starling A, Rocco P, Cambi F, Hobson GM, Passos Bueno MR, Zatz M (2002) Further evidence for a fourth gene causing X-linked pure spastic paraplegia. Am J Med Genet 111:152–156

3. Krantic S, Mechawar N, Reix S, Quirion R (2007) Apoptosis-inducing factor: a matter of neuron life and death. Prog Neurobiol 81(3):179–196 Feb

4. Kobayashi H, Hoffman EP, Marks HG (1994) The rumpshaker mutation in spastic paraplegia. Nat Genet 7(3):351–352, Jul

5. Fink JK (2003) The hereditary spastic paraplegias. Nine genes and counting. Arch Neurol 60:1045–1049

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