Hirschsprung disease as a yet undescribed phenotype in a patient withARID1Bmutation-Reference-Cited by-同舟云学术

Hirschsprung disease as a yet undescribed phenotype in a patient withARID1Bmutation

Author:

Takenouchi Toshiki¹²,Yoshihashi Hiroshi³,Sakaguchi Yuri²⁴,Uehara Tomoko¹,Honda Masataka⁵,Takahashi Takao²,Kosaki Kenjiro¹,Miyama Sahoko⁴

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 Genetics; Tokyo Metropolitan Children's Medical Center; Fuchu Tokyo Japan

4. Department of Neurology; Tokyo Metropolitan Children's Medical Center; Fuchu Tokyo Japan

5. Department of Nephrology; Tokyo Metropolitan Children's Medical Center; Fuchu Tokyo Japan

Funder

Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Keio University Research Grants for Life Science and Medicine

Japan Foundation for Pediatric Research

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference13 articles.

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