DCTN1 mutations in Perry syndrome-Reference-Cited by-同舟云学术

DCTN1 mutations in Perry syndrome

Published:2009-01-11 Issue:2 Volume:41 Page:163-165
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Farrer Matthew J,Hulihan Mary M,Kachergus Jennifer M,Dächsel Justus C,Stoessl A Jon,Grantier Linda L,Calne Susan,Calne Donald B,Lechevalier Bernard,Chapon Francoise,Tsuboi Yoshio,Yamada Tatsuo,Gutmann Ludwig,Elibol Bülent,Bhatia Kailash P,Wider Christian,Vilariño-Güell Carles,Ross Owen A,Brown Laura A,Castanedes-Casey Monica,Dickson Dennis W,Wszolek Zbigniew K

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.293.pdf

Reference13 articles.

1. Wider, C. & Wszolek, Z.K. Parkinsonism Relat. Disord. 14, 1–7 (2008).

2. Wider, C. et al. Parkinsonism Relat. Disord. advance online publication, doi: 10.1016/j.parkreldis.2008.07.005 (23 August 2008).

3. Ott, J. Proc. Natl. Acad. Sci. USA 86, 4175–4178 (1989).

4. Sobel, E., Sengul, H. & Weeks, D.E. Hum. Hered. 52, 121–131 (2001).

5. Schroer, T.A. Annu. Rev. Cell Dev. Biol. 20, 759–779 (2004).

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