✦ LIBER ✦

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

✍ Scribed by Sugawara, T.; Mazaki-Miyazaki, E.; Fukushima, K.; Shimomura, J.; Fujiwara, T.; Hamano, S.; Inoue, Y.; Yamakawa, K.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mosaic SCN1A Mutation in Familial Severe

✍ Carla Marini; Davide Mei; J. Helen Cross; Renzo Guerrini 📂 Article 📅 2006 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 244 KB

Recurrent De Novo Mutations of SCN1A in

✍ Jennifer A. Kearney; Anna K. Wiste; Ulrich Stephani; Michelle M. Trudeau; Anne S 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 147 KB

Novel SCN1A mutations in Indonesian pati

✍ Elisabeth Siti Herini; Gunadi; Marjan J.A. Van Kempen; Surini Yusoff; Sutaryo; S 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 339 KB

Significant correlation of the SCN1A mut

✍ Iori Ohmori; Mamoru Ouchida; Yoko Ohtsuka; Eiji Oka; Kenji Shimizu 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 229 KB

SCN1A Mutation Mosaicism in a Family wit

✍ Masafumi Morimoto; Emi Mazaki; Akira Nishimura; Tomohiro Chiyonobu; Yasuko Sawai 📂 Article 📅 2006 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 252 KB

Is phenotype difference in severe myoclo

✍ Iori Ohmori; Yoko Ohtsuka; Mamoru Ouchida; Tatsuya Ogino; Satoshi Maniwa; Kenji 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 201 KB