TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy-Reference-Cited by-同舟云学术

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Published:2008-10-26 Issue:11 Volume:40 Page:1288-1290
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Čížková Alena,Stránecký Viktor,Mayr Johannes A,Tesařová Markéta,Havlíčková Vendula,Paul Jan,Ivánek Robert,Kuss Andreas W,Hansíková Hana,Kaplanová Vilma,Vrbacký Marek,Hartmannová Hana,Nosková Lenka,Honzík Tomáš,Drahota Zdeněk,Magner Martin,Hejzlarová Kateřina,Sperl Wolfgang,Zeman Jiří,Houštěk Josef,Kmoch Stanislav

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.246.pdf

Reference14 articles.

1. Collinson, I.R., Skehel, J.M., Fearnley, I.M., Runswick, M.J. & Walker, J.E. Biochemistry 35, 12640–12646 (1996).

2. Ackerman, S.H. & Tzagoloff, A. Prog. Nucleic Acid Res. Mol. Biol. 80, 95–133 (2005).

3. Pickova, A., Potocky, M. & Houstek, J. Proteins 59, 393–402 (2005).

4. Wang, Z.G., White, P.S. & Ackerman, S.H. J. Biol. Chem. 276, 30773–30778 (2001).

5. Zeng, X., Neupert, W. & Tzagoloff, A. Mol. Biol. Cell 18, 617–626 (2007).

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