| 翻訳と辞書 |
| Naomichi Matsumoto ： ウィキペディア英語版 |
Naomichi Matsumoto
is a Japanese physician and medical geneticist who identified several causative genes for human diseases, including Sotos syndrome (2002), Marfan syndrome type II (2004), Ohtahara syndrome (2008), West syndrome (2010), Microphthalmia with limb anomalies (2011), Autosomal-recessive cerebellar ataxias (2011), Hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC) (2011), Porencephaly (2012), and Coffin-Siris syndrome (2012).
Matsumoto has been the editor-in-chief of the scientific journal ''Journal of Human Genetics'' since 2014.〔Matsumoto, N. (2014). "A message from the new Editor-in-Chief". ''Journal of Human Genetics'' 59: 1.〕
== Biography ==
Matsumoto was born in Saga Prefecture, Japan, and completed his M.D. in 1986 from Kyushu University School of Medicine.〔(CV at 10th INternational Workshop on Advanced Genomics )〕 After residency in obstetrics and gynecology at Kyushu University Hospital, he worked as an obstetrician and gynecologist for several years.〔 Wishing to pursue advanced study in medical genetics, he went to Nagasaki University to study as a graduate student under Norio Niikawa, who discovered Kabuki syndrome. He obtained his doctorate in genetics in 1997 from the same institution, before becoming a postdoctoral fellow at the University of Chicago.〔 He was appointed Professor and Chairman of the Department of Human Genetics at Yokohama City University School of Medicine in 2003.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
■ウィキペディアで「Naomichi Matsumoto」の詳細全文を読む
スポンサード リンク
| 翻訳と辞書 : 翻訳のためのインターネットリソース |
Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.
|
|