Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9

作者：Voraluck Phatarakijnirund, Steven Mumm, William H. McAlister, Deborah V. Novack, Deborah Wenkert, Karen L. Clements, Michael P. Whyte · 发表于：Bone · 年份：2015 · DOI：10.1016/j.bone.2015.11.022 · 被引用次数：63 · 研究领域：Ion channel regulation and function、Hereditary Neurological Disorders、Cardiac electrophysiology and arrhythmias