Title: | Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family |
Journal : | Journal of molecular medicine, 83 |
Authors: | Wang Q ; Liu M ; Xu C ; Tang Z ; Liao Y ; Du R ; Li W ; Wu X ; Wang X ; Liu P ; Zhang X ; Zhu J ; Ren X ; Ke T ; Yang J |
Material Type: | Article |
Publication Date: | 2005 |
Size: | p. 203-208 |
Languages: | English |
Keywords : | autosomal dominant inheritance ; calcium channels ; China ; familial hypokalemic periodic paralysis type 1 ; family trees ; genetic linkage ; genetic mutations ; heterozygotes ; molecular genetics ; muscle weakness ; penetrance ; potassium ; skeletal muscle |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15726306&query_hl=16 |