Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Epilepsy and HNRNPU[original query] |
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Diagnostic implications of genetic copy number variation in epilepsy plus. Epilepsia 2019 3 60 (4): 689-706. Coppola Antonietta, Cellini Elena, Stamberger Hannah, Saarentaus Elmo, Cetica Valentina, Lal Dennis, Djémié Tania, Bartnik-Glaska Magdalena, Ceulemans Berten, Helen Cross J, Deconinck Tine, Masi Salvatore De, Dorn Thomas, Guerrini Renzo, Hoffman-Zacharska Dorotha, Kooy Frank, Lagae Lieven, Lench Nicholas, Lemke Johannes R, Lucenteforte Ersilia, Madia Francesca, Mefford Heather C, Morrogh Deborah, Nuernberg Peter, Palotie Aarno, Schoonjans An-Sofie, Striano Pasquale, Szczepanik Elzbieta, Tostevin Anna, Vermeesch Joris R, Van Esch Hilde, Van Paesschen Wim, Waters Jonathan J, Weckhuysen Sarah, Zara Federico, De Jonghe Peter, Sisodiya Sanjay M, Marini Carla, , |
Clinical and genetic characteristics of patients with Doose syndrome. Epilepsia open 2020 9 5 (3): 442-450. Hinokuma Nodoka, Nakashima Mitsuko, Asai Hideyuki, Nakamura Kazuyuki, Akaboshi Shinjiro, Fukuoka Masataka, Togawa Masami, Oana Shingo, Ohno Koyo, Kasai Mariko, Ogawa Chikako, Yamamoto Kazuna, Okumiya Kiyohito, Chong Pin Fee, Kira Ryutaro, Uchino Shumpei, Fukuyama Tetsuhiro, Shinagawa Tomoe, Miyata Yohane, Abe Yuichi, Hojo Akira, Kobayashi Kozue, Maegaki Yoshihiro, Ishikawa Nobutsune, Ikeda Hiroko, Amamoto Masano, Mizuguchi Takeshi, Iwama Kazuhiro, Itai Toshiyuki, Miyatake Satoko, Saitsu Hirotomo, Matsumoto Naomichi, Kato Mitsuhi |
The role of copy number variants in the genetic architecture of common familial epilepsies. Epilepsia 2023 12 . Authors are not available |
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