Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy-Reference-Cited by-同舟云学术

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Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy

Published:2014-04-01 Issue:16 Volume:23 Page:4249-4259
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Boyer Justin G.,Deguise Marc-Olivier,Murray Lyndsay M.,Yazdani Armin,De Repentigny Yves,Boudreau-Larivière Céline,Kothary Rashmi

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/23/16/4249/13923374/ddu142.pdf

Reference31 articles.

1. The many faces of SMN: deciphering the function critical to spinal muscular atrophy pathogenesis;Boyer;Future Neurol.,2010

2. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals;Hahnen;Hum. Mol. Genet.,1995

3. Identification and characterization of a spinal muscular atrophy-determining gene;Lefebvre;Cell,1995

4. Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?;Burghes;Nat. Rev. Neurosci.,2009

5. SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens;Rochette;Hum. Genet.,2001

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