Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia-Reference-Cited by-同舟云学术

Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia

Author:

Takenouchi Toshiki¹²,Okamoto Nobuhiko³,Ida Shinobu⁴,Uehara Tomoko¹,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 Medical Genetics; Osaka Medical Center and Research Institute for Maternal and Child Health; Osaka Japan

4. Department of Gastroenterology and Endocrinology; Osaka Medical Center and Research Institute for Maternal and Child Health; Osaka Japan

Funder

Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Keio University Research Grants

Japan Foundation for Pediatric Research

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference9 articles.

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