CNOT2 haploinsufficiency causes a neurodevelopmental disorder with characteristic facial features

Tomoko Uehara, Takatoshi Tsuchihashi, Mamiko Yamada, Hisato Suzuki, Toshiki Takenouchi, Kenjiro Kosaki

研究成果: Letter

元の言語English
ジャーナルAmerican Journal of Medical Genetics, Part A
DOI
出版物ステータスAccepted/In press - 2019 1 1

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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