Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and CHRNE[original query] |
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Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. The application of clinical genetics 2016 9 39-47. Marshall-Gradisnik Sonya, Huth Teilah, Chacko Anu, Johnston Samantha, Smith Pete, Staines Dona |
Congenital myasthenic syndrome in Israel: Genetic and clinical characterization. Neuromuscular disorders : NMD 2016 12 27 (2): 136-140. Aharoni Sharon, Sadeh Menachem, Shapira Yehuda, Edvardson Simon, Daana Muhannad, Dor-Wollman Talia, Mimouni-Bloch Aviva, Halevy Ayelet, Cohen Rony, Sagie Liora, Argov Zohar, Rabie Malcolm, Spiegel Ronen, Chervinsky Ilana, Orenstein Naama, Engel Andrew G, Nevo Yor |
Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort. Journal of clinical neuromuscular disease 2018 Sep 20 (1): 14-27. Selvam Pavalan, Arunachal Gautham, Danda Sumita, Chapla Aaron, Sivadasan Ajith, Alexander Mathew, Thomas Maya Mary, Thomas Nihal |
A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology 2018 2 265 (3): 708-713. Estephan Eduardo de Paula, Sobreira Cláudia Ferreira da Rosa, Dos Santos André Clériston José, Tomaselli Pedro José, Marques Wilson, Ortega Roberta Paiva Magalhães, Costa Marcela Câmara Machado, da Silva André Macedo Serafim, Mendonça Rodrigo Holanda, Caldas Vitor Marques, Zambon Antonio Alberto, Abath Neto Osório, Marchiori Paulo Eurípedes, Heise Carlos Otto, Reed Umbertina Conti, Azuma Yoshiteru, Töpf Ana, Lochmüller Hanns, Zanoteli Edm |
No Hot Spot Mutations CHRNE c.1327 delG, CHAT c.914T>C, and RAPSN c.264C>A in Iranian Patients with Congenital Myasthenic Syndrome. Iranian journal of child neurology 2019 5 13 (2): 135-143. Parvizi Omran Sima, Houshmand Massod, Dominic Donkor, Farjami Zahra, Karimzadeh Parvan |
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