Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome-Reference-Cited by-同舟云学术

Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome

Published:2019-01-03 Issue:1 Volume:20 Page:9-25
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Borna Nurun Nahar,Kishita Yoshihito,Kohda Masakazu,Lim Sze Chern,Shimura Masaru,Wu Yibo,Mogushi Kaoru,Yatsuka Yukiko,Harashima Hiroko,Hisatomi Yuichiro,Fushimi Takuya,Ichimoto Keiko,Murayama Kei,Ohtake Akira,Okazaki Yasushi

Funder

MEXT-Supported Program for the Private University Research Branding Project

Japan Agency for Medical Research and Development

Uehara Memorial Foundation

Japan Society for the Promotion of Science

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-018-0561-9.pdf

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3. Rackham O, Mercer TR, Filipovska A (2012) The human mitochondrial transcriptome and the RNA-binding proteins that regulate its expression. Wiley Interdiscip Rev RNA 3(5):675–695. https://doi.org/10.1002/wrna.1128

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