Deficiency of mitochondrial ATP synthase of nuclear genetic origin-Reference-Cited by-同舟云学术

Deficiency of mitochondrial ATP synthase of nuclear genetic origin

Published:2006-12 Issue:12 Volume:16 Page:821-829
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Sperl W.,Ješina P.,Zeman J.,Mayr J.A.,DeMeirleir L.,VanCoster R.,Pícková A.,Hansíková H.,Houšt’ková H.,Krejčík Z.,Koch J.,Smet J.,Muss W.,Holme E.,Houštěk J.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference31 articles.

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2. Nuclear genetic defects of oxidative phosphorylation;Shoubridge;Hum Mol Genet,2001

3. Mitochondrial diseases and ATPase defects of nuclear origin;Houstek;Biochim Biophys Acta,2004

4. The role of the stalk in the coupling mechanism of F1F0-ATPases;Walker;FEBS Lett,1994

5. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

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