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 journalLetterpeer-review

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)2506-2509
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Issue number12
Publication statusPublished - 2019 Dec 1

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this