Title: | Human skeletal muscle sodium channelopathies |
Journal : | Neurological sciences, 26, 4 |
Authors: | Vicart S ; Sternberg D ; Fontaine B ; Meola G |
Material Type: | Article |
Publication Date: | 2005 |
Size: | p. 194-202 |
Languages: | English |
Keywords : | congenital myasthenic syndrome ; diagrams ; familial periodic paralysis ; genetic mutations ; molecular genetics ; myasthenia gravis ; myotonic syndrome ; review article ; SCN4A gene ; skeletal muscle ; sodium channel disease |
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=16193245&query_hl=18&itool=pubmed_docsum |