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pro vyhledávání: '"Mari Maeno"'
Autor:
Ayumi Matsumoto, Sumimasa Yamashita, Kenji Sugai, Kazuyuki Nakamura, Kayoko Saito, Mari Maeno, Taku Nakagawa, Kiyomi Nishiyama, Hiroshi Arai, Yoshinobu Oyazato, Ryosuke Kusano, Kaoru Imai, Naomichi Matsumoto, Takanori Yamagata, Shelly K. Weiss, Tami Uster, Hirofumi Kodera, Hirofumi Kashii, Kiyoshi Hayasaka, Noriko Miyake, Mitsuhiro Kato, Hirotomo Saitsu, Yoshinori Tsurusaki, Mitsuko Nakashima, Takanari FujII, David Chitayat, Masaya Kubota
Publikováno v:
Epilepsia. 54:1282-1287
Summary Purpose KCNQ2 mutations have been found in patients with benign familial neonatal seizures, myokymia, or early onset epileptic encephalopathy (EOEE). In this study, we aimed to delineate the clinical spectrum of EOEE associated with KCNQ2 mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a018ee80cb36e02bf4816c46478271
https://doi.org/10.1111/epi.12200
https://doi.org/10.1111/epi.12200
