De la levure aux maladies neurodégénératives-Reference-Cited by-同舟云学术

De la levure aux maladies neurodégénératives

Published:2010-10 Issue:10 Volume:26 Page:836-841
ISSN:0767-0974
Container-title:médecine/sciences
language:
Short-container-title:Med Sci (Paris)

Author:

Lenaers Guy,Amati-Bonneau Patrizia,Delettre Cécile,Chevrollier Arnaud,Verny Christophe,Miléa Dan,Procaccio Vincent,Bonneau Dominique,Hamel Christian,Reynier Pascal

Publisher

EDP Sciences

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.medecinesciences.org/10.1051/medsci/20102610836/pdf

Reference36 articles.

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2. Alexander C, Votruba M, Pesch UE,et al. OPA1, encoding a dynaminrelated GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.Nat Genet2000 ; 26 : 211-5.

3. Zuchner S, Mersiyanova IV, Muglia M,et al. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.Nat Genet2004 ; 36 : 449-51.

4. Waterham HR, Koster J, Van Roermund CW,et al. A lethal defect of mitochondrial and peroxisomal fission.N Eng J Med2007 ; 356 : 1736-41.

5. Baxter RV, Ben Othmane K, Rochelle JM,et al. Ganglioside-induced differentiation-associated protein1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.Nat Genet2002 ; 30 : 21-2.

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