المؤلفون: Masakazu Kohda, Yoshimi Tokuzawa, Yoshihito Kishita, Hiromi Nyuzuki, Yohsuke Moriyama, Yosuke Mizuno, Tomoko Hirata, Yukiko Yatsuka, Yzumi Yamashita-Sugahara, Yutaka Nakachi, Hidemasa Kato, Akihiko Okuda, Shunsuke Tamaru, Nurun Nahar Borna, Kengo Banshoya, Toshiro Aigaki, Yukiko Sato-Miyata, Kohei Ohnuma, Tsutomu Suzuki, Asuteka Nagao, Hazuki Maehata, Fumihiko Matsuda, Koichiro Higasa, Masao Nagasaki, Jun Yasuda, Masayuki Yamamoto, Takuya Fushimi, Masaru Shimura, Keiko Kaiho-Ichimoto, Hiroko Harashima, Taro Yamazaki, Masato Mori, Kei Murayama, Akira Ohtake, Yasushi Okazaki

المصدر: PLoS Genetics, Vol 12, Iss 1, p e1005679 (2016)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC4704781?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/158105bef6724bed92af4dd632668bf3

المؤلفون: Masaru Shimura, Hiromi Nyuzuki, Tsutomu Suzuki, Yoshihito Kishita, Kengo Banshoya, Keiko Kaiho-Ichimoto, Masato Mori, Jun Yasuda, Masao Nagasaki, Shunsuke Tamaru, Taro Yamazaki, Takuya Fushimi, Kei Murayama, Yutaka Nakachi, Toshiro Aigaki, Koichiro Higasa, Tomoko Hirata, Fumihiko Matsuda, Yohsuke Moriyama, Akira Ohtake, Masakazu Kohda, Yoshimi Tokuzawa, Akihiko Okuda, Yukiko Sato-Miyata, Yzumi Yamashita-Sugahara, Yosuke Mizuno, Yukiko Yatsuka, Kohei Ohnuma, Nurun Nahar Borna, Hiroko Harashima, Yasushi Okazaki, Masayuki Yamamoto, Hidemasa Kato, Asuteka Nagao, Hazuki Maehata

المصدر: PLoS Genetics, Vol 12, Iss 1, p e1005679 (2016)
PLoS Genetics

مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, Mitochondrial DNA, Mitochondrial Diseases, Adolescent, lcsh:QH426-470, Mitochondrial disease, Biology, Gene mutation, DNA, Mitochondrial, Polymorphism, Single Nucleotide, 03 medical and health sciences, Genetic Heterogeneity, 0302 clinical medicine, INDEL Mutation, Genetics, medicine, Humans, Exome, Child, Molecular Biology, Gene, Genetics (clinical), Ecology, Evolution, Behavior and Systematics, Chromosome Aberrations, Genetic heterogeneity, Respiratory chain complex, Infant, Newborn, High-Throughput Nucleotide Sequencing, Infant, Fibroblasts, medicine.disease, Mitochondria, lcsh:Genetics, 030104 developmental biology, Mitochondrial respiratory chain, Child, Preschool, Female, 030217 neurology & neurosurgery, Research Article

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a23d3e627df8fca34ee39cd9fb83a8
http://europepmc.org/articles/PMC4704781?pdf=render