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

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Haploinsufficiency
Neurodevelopmental Disorders

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

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title = "CNOT2 haploinsufficiency causes a neurodevelopmental disorder with characteristic facial features",
author = "Tomoko Uehara and Takatoshi Tsuchihashi and Mamiko Yamada and Hisato Suzuki and Toshiki Takenouchi and Kenjiro Kosaki",
year = "2019",
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journal = "American Journal of Medical Genetics, Part A",
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AU - Uehara, Tomoko

AU - Tsuchihashi, Takatoshi

AU - Yamada, Mamiko

AU - Suzuki, Hisato

AU - Takenouchi, Toshiki

AU - Kosaki, Kenjiro

PY - 2019/1/1

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JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

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