Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Epilepsy and RYR2[original query] |
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Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
Biallelic ADGRV1 variants are associated with Rolandic epilepsy. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 6 43 (2): 1365-1374. Liu Zhigang, Ye Xingguang, Zhang Jieyan, Wu Benze, Dong Shiwei, Gao Pingmi |
RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia. Frontiers in neuroscience 2021 4 15 629610. Ma Mei-Gang, Liu Xiao-Rong, Wu Yuan, Wang Jie, Li Bing-Mei, Shi Yi-Wu, Su Tao, Li Bin, Liu De-Tian, Yi Yong-Hong, Liao Wei-Pi |
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca regulation. Proceedings of the National Academy of Sciences of the United States of America 2021 12 118 (52): . Halvorsen Matthew, Gould Laura, Wang Xiaohan, Grant Gariel, Moya Raquel, Rabin Rachel, Ackerman Michael J, Tester David J, Lin Peter T, Pappas John G, Maurano Matthew T, Goldstein David B, Tsien Richard W, Devinsky Orr |
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- Page last updated:Apr 22, 2024
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