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[2AW-17-7] Validation and diagnosis of novel variants of mitochondrial diseases associated with the ECHS1 gene

Yoshihito Kishita1, Ayumu Sugiura2, Takanori Onuki3, Tomohiro Ebihara4, Tetsuro Matsuhashi3, Masaru Shimura3, Takuya Fushimi3, Noriko Ichino2, Yoshie Nagatakidani1, Hitomi Nishihata1, Kazuhiro R Nitta2, Yukiko Yatsuka2, Atsuko ImaiOkazaki2, Yibo Wu5,6, Hitoshi Osaka7, Akira Ohtake8,9, Kei Murayama3,10, Yasushi Okazaki11,2 (1.Dept. of Life Sci., Fac. of Sci. and Eng., Kindai Univ., 2.Diag. & Therap. of Intractable Dis. Intractable Dis. Res. Cent., Juntendo Univ., 3.Dept. of Metab., Chiba Children's Hosp., 4.Dept. of Neonat., Chiba Children's Hosp., 5.YCI Lab. for Next-Gen. Proteomics, RIKEN Cent. of Integrative Med. Sci., 6.Univ. of Geneva, Sciences II, 7.Dept. of Pediatr., Jichi Med. Univ., 8.Dept. of Pediatr. & Clin. Genomics, Fac. of Med., Saitama Med. Univ., 9.Cent. for Intractable Dis., Saitama Med. Univ. Hosp., 10.Cent. for Med. Genetics, Chiba Children's Hosp., 11.Lab. for Comprehensive Genomic Anal., RIKEN Cent. for Integrative Med. Sci.)

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