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Naomichi Matsumoto (松本 直通, Matsumoto Naomichi, born August 3, 1961) 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).

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  • Naomichi Matsumoto (松本 直通, Matsumoto Naomichi, born August 3, 1961) 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. (en)
  • 松本 直通(まつもと なおみち、1961年8月3日 - )は、日本の医学者。博士(医学)(長崎大学、1997年)。専門は遺伝学。横浜市立大学大学院医学研究科教授。 ソトス症候群を含む多くの神経系疾患の責任遺伝子を見出した。素晴らしい学問的な功績に加えて、後進の指導にも優れた研究者である。またコーヒーにも造詣が深い。 (ja)
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  • 1961-08-03 (xsd:date)
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  • 松本 直通 (en)
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  • 1961-08-03 (xsd:date)
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  • Saga Prefecture, Japan (en)
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  • Naomichi Matsumoto (en)
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  • Japanese (en)
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  • 松本 直通 (en)
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  • ja (en)
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  • 松本 直通(まつもと なおみち、1961年8月3日 - )は、日本の医学者。博士(医学)(長崎大学、1997年)。専門は遺伝学。横浜市立大学大学院医学研究科教授。 ソトス症候群を含む多くの神経系疾患の責任遺伝子を見出した。素晴らしい学問的な功績に加えて、後進の指導にも優れた研究者である。またコーヒーにも造詣が深い。 (ja)
  • Naomichi Matsumoto (松本 直通, Matsumoto Naomichi, born August 3, 1961) 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). (en)
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  • 松本直通 (ja)
  • Naomichi Matsumoto (en)
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