Classic Rett syndrome in a boy with R133C mutation of MECP2

Autor:	Masuyama, Tatsuo1 ssgmasubb@yahoo.co.jp, Matsuo, Muneaki1, Jing, Jin J.2, Tabara, Yasuharu2, Kitsuki, Kyoko1, Yamagata, Hidehisa2, Kan, Yuka1, Miki, Tetsuro3, Ishii, Kiyohisa1, Kondo, Ikuko2
Zdroj:	Brain & Development. Sep2005, Vol. 27 Issue 6, p439-442. 4p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu Full Text from ScienceDirect