About this Biochemistry, Genetics and Molecular Biology article
Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy by Iwama, Kazuhiro; Takaori, Toru; Fukushima, Ai; Tohyama, Jun; Ishiyama, Akihiko; Ohba, Chihiro; Mitsuhashi, Satomi; Miyatake, Satoko; Takata, Atsushi; Miyake, Noriko; Ito, Shuichi; Saitsu, Hirotomo; Mizuguchi, Takeshi; Matsumoto, Naomichi is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Iwama, Kazuhiro; Takaori, Toru; Fukushima, Ai; Tohyama, Jun; Ishiyama, Akihiko; Ohba, Chihiro; Mitsuhashi, Satomi; Miyatake, Satoko; Takata, Atsushi; Miyake, Noriko; Ito, Shuichi; Saitsu, Hirotomo; Mizuguchi, Takeshi; Matsumoto, Naomichi
- Publisher
- Nature Publishing Group; Springer Science and Business Media LLC; Springer Verlag (ISSN 1435-232X)
- Published
- 2018
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)