ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency-Reference-Cited by-同舟云学术

ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency

Published:2008-03 Issue:3 Volume:82 Page:661-672
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lagier-Tourenne Clotilde,Tazir Meriem,López Luis Carlos,Quinzii Catarina M.,Assoum Mirna,Drouot Nathalie,Busso Cleverson,Makri Samira,Ali-Pacha Lamia,Benhassine Traki,Anheim Mathieu,Lynch David R.,Thibault Christelle,Plewniak Frédéric,Bianchetti Laurent,Tranchant Christine,Poch Olivier,DiMauro Salvatore,Mandel Jean-Louis,Barros Mario H.,Hirano Michio,Koenig Michel

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference37 articles.

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5. Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations;Winterthun;Neurology,2005

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