SMN oligomerization defect correlates with spinal muscular atrophy severity-Reference-Cited by-同舟云学术

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SMN oligomerization defect correlates with spinal muscular atrophy severity

Published:1998-05 Issue:1 Volume:19 Page:63-66
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lorson Christian L.,Strasswimmer John,Yao Jun-Mei,Baleja James D.,Hahnen Eric,Wirth Brunhilde,Le Thanh,Burghes Arthur H.M.,Androphy Elliot J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0598-63.pdf

Reference25 articles.

1. Lefebvre, S. et al. Identification and characterization of a spinal muscular atrophy determining gene. Cell 80, 155–165 (1995).

2. Brzustowicz, L.M. et al. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3. Nature 344, 540–541 (1990).

3. Melki, J. et al. Gene for chronic spinal muscular atrophies maps to chromosome 5q. Nature 344, 767–768 (1990).

4. Burghes, A. When is a deletion not a deletion?When it is converted. Am. J. Hum. Genet. 61, 9–15 (1997).

5. Melki, J. Spinal muscular atrophy. Curr. Opin. Neurol. 10, 381–385 (1997).

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