Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy
暂无分享,去创建一个
A. Konagaya | H. Kurahashi | T. Kojima | H. Oguni | S. Kure | J. Natsume | T. Okuno | S. Kaneko | S. Yasumoto | S. Hirose | A. Ishii | Takahito Inoue | Y. Shirasaka | M. Ohfu | Aki Hasegawa | Masatoshi Ito | Ji-wen Wang | T. Fujii | A. Ogawa