CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome-Reference-Cited by-同舟云学术

CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome

Author:

Uehara Tomoko¹^ORCID,Takenouchi Toshiki¹²^ORCID,Yamaguchi Yu¹³,Daimon Yumi¹⁴,Suzuki Hisato¹,Sakaguchi Yuri¹^ORCID,Kosaki Kenjiro¹

Affiliation:

1. Center for Medical Genetics; Keio University School of Medicine; Tokyo Japan

2. Department of Pediatrics; Keio University School of Medicine; Tokyo Japan

3. Department of Clinial Genetics; Gunma Children's Medical Center; Gunma Japan

4. Department of Pediatrics; Hino Municipal Hospital; Tokyo Japan

Funder

Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference20 articles.

5. The CCR4-NOT complex plays diverse roles in mRNA metabolism;Denis;Progress in Nucleic Acid Research and Molecular Biology,2003

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