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Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review

机译：SCN4A基因突变引起的周期性麻痹和先天性肌强直重叠重叠两个家族报道及文献复习

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期刊名称 Channels
作者
Shan Huang; Wei Zhang; Xueli Chang; Junhong Guo;
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作者单位

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年(卷),期 2015(13),1
年度 2015
页码 110–119
总页数 10
原文格式 PDF
正文语种
中图分类分子生物学;
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1. Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review [J] . Shan Huang, Wei Zhang, Xueli Chang, Channels . 2019,第1期

机译：SCN4A基因突变引起的周期性麻痹和先天性肌强直重叠重叠两个家族报道及文献复习
2. Hyperkalemic periodic paralysis and paramyotonia congenita caused by a de novo mutation in the SCN4A gene [J] . GM Lee, JB Kim Neurology Asia . 2011,第2011期

机译：SCN4A基因从头突变引起的高钾性周期性麻痹和先天性肌强直
3. Hyperkalemic periodic paralysis and paramyotonia congenita caused by a de novo mutation in the SCN4A gene [J] . GM Lee, JB Kim Neurological Journal of South East Asia . 2011,第2期

机译：SCN4A基因从头突变引起的高钾性周期性麻痹和先天性肌强直
4. UGT1A1 gene mutation and hyperthyroidism combined with hepatic failure: case report and literature review [C] . Qianyu Yan, Jingyun Fu International Conference on Biological Information and Biomedical Engineering . 2019

机译：UGT1A1基因突变和甲状腺功能亢进结合肝衰竭：案例报告和文献综述
5. Mouse Models of Periodic Paralysis in Andersen Tawil Syndrome and Functional Studies of Novel Nav1.4 Mutations in Myotonia & Myopathy [D] . ?Elia, Nathaniel Curtis 2020

机译：安德森三伐综合征治疗术后瘫痪的小鼠模型和新型NAV1.4突变术中的肌疗法突变功能研究
6. Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A [O] . 2004

机译：严重的婴儿高钾血症性周期性麻痹和先天性肌强直：拓宽与SCN4A中T704M突变相关的临床范围
7. Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A [O] . 2003

机译：严重的婴儿高钾血症性周期性麻痹和先天性肌强直：拓宽与SCN4A中T704M突变相关的临床范围

Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review

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