Genotype-phenotype correlation and therapeutic rationale in Hyperkalemic periodic paralysis

Erstveröffentlichung
2007Authors
Jurkat-Rott, Karin
Lehmann-Horn, Frank
Wissenschaftlicher Artikel
Published in
Neurotherapeutics ; 4 (2007), 2. - S. 216-224. - ISSN 1933-7213
Link to publication
https://dx.doi.org/10.1016/j.nurt.2007.02.001Faculties
Medizinische FakultätInstitutions
Institut für Angewandte PhysiologieSubject headings
[Free subject headings]: hyperkalemic periodic paralysis | myotonia | hypokalemic periodic paralysis | Andersen-Tawil syndrome | voltage-gated sodium channel | channelopathies | muscle sodium-channel | adynamia episodica hereditaria | paramyotonia-congenita | skeletal-muscle | andersens-syndrome | slow inactivation | alpha-subunit | cardiac-arrhythmia | kcnj2 mutations[DDC subject group]: DDC 610 / Medicine & health