Autosomal dominant monosymptomatic myotonia permanens

scientific article published on 01 July 2006

Autosomal dominant monosymptomatic myotonia permanens is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1212/01.WNL.0000223838.88872.DA
P698PubMed publication ID16832098

P2093author name stringMorten Duno
John Vissing
Eskild Colding-Jørgensen
P433issue1
P921main subjectmyotonia permanensQ56014436
P304page(s)153-155
P577publication date2006-07-01
P1433published inNeurologyQ1161692
P1476titleAutosomal dominant monosymptomatic myotonia permanens
P478volume67

Reverse relations

cites work (P2860)
Q43199994Dramatic improvement of myotonia permanens with flecainide: a two-case report of a possible bench-to-bedside pharmacogenetics strategy
Q34523030Muscle channelopathies: the nondystrophic myotonias and periodic paralyses
Q55285566Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life.
Q26747746Myotonic disorders: A review article
Q35106208Sodium and chloride channelopathies with myositis: coincidence or connection?
Q33570009The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.
Q36774714The nondystrophic myotonias
Q27347910Translational approach to address therapy in myotonia permanens due to a new SCN4A mutation