Coenzyme Q10-responsive ataxia: 2-year-treatment follow-up-Reference-Cited by-同舟云学术

Coenzyme Q10-responsive ataxia: 2-year-treatment follow-up

Published:2010-04-13 Issue:9 Volume:25 Page:1262-1268
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Pineda Merce,Montero Raquel,Aracil Asuncion,O'Callaghan Mar M.,Mas Ana,Espinos Carmen,Martinez-Rubio Dolores,Palau Francesc,Navas Placido,Briones Paz,Artuch Rafael

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference14 articles.

1. Cerebellar ataxia and coenzyme Q10 deficiency;Lamperti;Neurology,2003

2. A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency;Quinzii;Am J Hum Genet,2006

3. Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders;Mollet;J Clin Invest,2007

4. Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations;López;Am J Hum Genet,2006

5. ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency;Lagier-Tourenne;Am J Hum Genet,2008

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