CNOT2 haploinsufficiency causes a neurodevelopmental disorder with characteristic facial features

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

Research output: Contribution to journalLetter

Original languageEnglish
JournalAmerican Journal of Medical Genetics, Part A
DOIs
Publication statusAccepted/In press - 2019 Jan 1

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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