Novel SIN3A mutation identified in a Japanese patient with Witteveen-Kolk syndrome期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Novel SIN3A mutation identified in a Japanese patient with Witteveen-Kolk syndrome

Authors:	Yoko Narumi-Kishimoto Naomi Araki Ohsuke Migita Tomoko Kawai Kohji Okamura Kazuhiko Nakabayashi Tadashi Kaname Yuri Ozawa Hiroshi Ozawa Fumio Takada Kenichiro Hata

Affiliation:	1. Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, Japan;2. Medical Genome Center, National Research Institute for Child Health and Development, Tokyo, Japan;3. Department of Medical Genetics, Kitasato University, Sagamihara, Japan;4. Department of Neuro-pediatrics, Shimada Ryouiku Center Hachiouji, Tokyo, Japan;5. Department of Pediatrics, St. Marianna University School of Medicine, Kawasaki, Japan;6. Department of Systems BioMedicine, National Research Institute for Child Health and Development, Tokyo, Japan;7. Department of Genome Medicine, National Research Institute for Child Health and Development, Tokyo, Japan

Abstract:

Keywords:	Corresponding author. Medecal Genome Center National Research Institute for Child Health and Development 2-10-1 Okura Setagaya Tokyo 157-8535 Japan.
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