Ontology highlight
ABSTRACT:
SUBMITTER: Chauveau C
PROVIDER: S-EPMC3954110 | biostudies-literature | 2014 Feb
REPOSITORIES: biostudies-literature
Chauveau Claire C Bonnemann Carsten G CG Julien Cedric C Kho Ay Lin AL Marks Harold H Talim Beril B Maury Philippe P Arne-Bes Marie Christine MC Uro-Coste Emmanuelle E Alexandrovich Alexander A Vihola Anna A Schafer Sebastian S Kaufmann Beth B Medne Livija L Hübner Norbert N Foley A Reghan AR Santi Mariarita M Udd Bjarne B Topaloglu Haluk H Moore Steven A SA Gotthardt Michael M Samuels Mark E ME Gautel Mathias M Ferreiro Ana A
Human molecular genetics 20131008 4
Core myopathies (CM), the main non-dystrophic myopathies in childhood, remain genetically unexplained in many cases. Heart disease is not considered part of the typical CM spectrum. No congenital heart defect has been reported, and childhood-onset cardiomyopathy has been documented in only two CM families with homozygous mutations of the TTN gene. TTN encodes titin, a giant protein of striated muscles. Recently, heterozygous TTN truncating mutations have also been reported as a major cause of do ...[more]