Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis

OBJECTIVE: To determine the motor-behavioral and neural correlates of putative functional common variants in the sodium-channel Na(V)1.8 encoding gene (SCN10A) in vivo in patients with multiple sclerosis (MS). METHODS: We recruited 161 patients with relapsing-onset MS and 94 demographically comparab...

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書誌詳細
出版年:Neurology
主要な著者: Roostaei, Tina, Sadaghiani, Shokufeh, Park, Min Tae M., Mashhadi, Rahil, Nazeri, Aria, Noshad, Sina, Salehi, Mohammad Javad, Naghibzadeh, Maryam, Moghadasi, Abdorreza Naser, Owji, Mahsa, Doosti, Rozita, Taheri, Amir Pejman Hashemi, Rad, Ali Shakouri, Azimi, Amirreza, Chakravarty, M. Mallar, Voineskos, Aristotle N., Nazeri, Arash, Sahraian, Mohammad Ali
フォーマット: Artigo
言語:Inglês
出版事項: Lippincott Williams & Wilkins 2016
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4773947/
https://ncbi.nlm.nih.gov/pubmed/26740675
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000002326
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