Cargando…
Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis
INTRODUCTION: Periodic paralyses (PP) are recurrent episodes of flaccid limb muscle weakness. Next to autosomal dominant forms, sporadic PP (SPP) cases are known but their genetics are unclear. METHODS: In a patient with hypokalemic SPP, we performed exome sequencing to identify a candidate gene. We...
Autores principales: | FAN, CHUNXIANG, KUHN, MARIUS, MBIOL, ALEXANDER PEPLER, GROOME, JAMES, WINSTON, VERN, BISKUP, SASKIA, LEHMANN-HORN, FRANK, JURKAT-ROTT, KARIN |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pacini Editore srl
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390110/ https://www.ncbi.nlm.nih.gov/pubmed/30838349 |
Ejemplares similares
-
Na(V)1.4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery
por: Groome, James R., et al.
Publicado: (2014) -
Na(V)1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers
por: Bayless-Edwards, Landon, et al.
Publicado: (2018) -
Domain III S4 in closed-state fast inactivation: Insights from a periodic paralysis mutation
por: Groome, James R, et al.
Publicado: (2014) -
Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation
por: Fan, Chunxiang, et al.
Publicado: (2013) -
Myocardial Infarction and AGT p.Thr174Met Polymorphism: A Meta-Analysis of 7657 Subjects
por: Li, Yan-yan, et al.
Publicado: (2021)