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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Nondystrophic Myotonia[original query]
Low-rate repetitive nerve stimulation protocol in an Italian cohort of patients affected by recessive myotonia congenita.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 2011 1 28 (1): 39-44.
Modoni Anna, D'Amico Adele, Dallapiccola Bruno, Mereu Maria Lucia, Merlini Luciano, Pagliarani Serena, Pisaneschi Elisa, Silvestri Gabriella, Torrente Isabella, Valente Enza Maria, Lo Monaco Mau
Sequence CLCN1 and SCN4A genes in patients with nondystrophic myotonia in Chinese people.
Medicine 2022 7 101 (29): e29591.
Meng Yan-Xin, Yu Mei, Liu Chunmiao, Zhang Haijuan, Yang Yuxiu, Zhang Ji
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