Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease-Reference-Cited by-同舟云学术

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Published:2005-01-30 Issue:3 Volume:37 Page:289-294
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Züchner Stephan,Noureddine Maher,Kennerson Marina,Verhoeven Kristien,Claeys Kristl,Jonghe Peter De,Merory John,Oliveira Sofia A,Speer Marcy C,Stenger Judith E,Walizada Gina,Zhu Danqing,Pericak-Vance Margaret A,Nicholson Garth,Timmerman Vincent,Vance Jeffery M

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1514.pdf

Reference27 articles.

1. Verhoeven, K. et al. Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1. Am. J. Hum. Genet. 69, 889–894 (2001).

2. Kennerson, M.L. et al. Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2. Am. J. Hum. Genet. 69, 883–888 (2001).

3. Jordanova, A. et al. Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35. Am. J. Hum. Genet. 73, 1423–1430 (2003).

4. Hinshaw, J.E. Dynamin and its role in membrane fission. Annu. Rev. Cell Dev. Biol. 16, 483–519 (2000).

5. Vance, J.M. The many faces of Charcot-Marie-Tooth disease. Arch. Neurol. 57, 638–640 (2000).

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