Author Correction: Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan
Guardado en:
Autores principales: | Nana Akiyama, Masaru Shimura, Taro Yamazaki, Hiroko Harashima, Takuya Fushimi, Tomoko Tsuruoka, Tomohiro Ebihara, Keiko Ichimoto, Ayako Matsunaga, Megumi Saito-Tsuruoka, Yukiko Yatsuka, Yoshihito Kishita, Masakazu Kohda, Akira Namba, Yoshimasa Kamei, Yasushi Okazaki, Shinji Kosugi, Akira Ohtake, Kei Murayama |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/70a42ea93a774ef6885c77b549ac60e9 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan
por: Nana Akiyama, et al.
Publicado: (2021) -
A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome
por: Yoshihito Kishita, et al.
Publicado: (2021) -
A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
por: Kazumichi Ota, et al.
Publicado: (2021) -
Development of a novel chronic kidney disease mouse model to evaluate the progression of hyperphosphatemia and associated mineral bone disease
por: Takashi Tani, et al.
Publicado: (2017) -
Lipopolysaccharide directly inhibits bicarbonate absorption by the renal outer medullary collecting duct
por: Shuichi Tsuruoka, et al.
Publicado: (2020)