Human Genome Epidemiology Literature Finder
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Query Trace: Syndrome and CACNA1G[original query] |
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De novo CACNA1G variants in developmental delay and early-onset epileptic encephalopathies. Journal of the neurological sciences 2020 8 416 117047. Kunii Misako, Doi Hiroshi, Hashiguchi Shunta, Matsuishi Toyojiro, Sakai Yasunari, Iai Mizue, Okubo Masaki, Nakamura Haruko, Takahashi Keita, Katsumoto Atsuko, Tada Mikiko, Takeuchi Hideyuki, Ishikawa Taro, Miyake Noriko, Saitsu Hirotomo, Matsumoto Naomichi, Tanaka Fumia |
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