Classic Rett syndrome in a boy with R133C mutation of MECP2

Brain and Development - Tập 27 - Trang 439-442 - 2005
Tatsuo Masuyama1, Muneaki Matsuo1, Jin J. Jing2, Yasuharu Tabara2, Kyoko Kitsuki1, Hidehisa Yamagata2, Yuka Kan1, Tetsuro Miki3, Kiyohisa Ishii1, Ikuko Kondo2
1Department of Pediatrics, Faculty of Medicine, Saga University, Saga, Japan
2Department of Medical Genetics, Ehime University School of Medicine, Ehime, Japan
3Department of Geriatric Medicine, Ehime University School of Medicine, Ehime, Japan

Tài liệu tham khảo

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