A new c.1621 C>G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis) : genotype-phenotype correlation
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-01-01
著者
-
Ploski Rafal
Department Of Medical Genetics Centre Of Biostructure Medical University Of Warsaw
-
Malek Lukasz
Department Of Interventlonal Cardiology And Angiology Institute Of Cardiology
-
LABIB Sarah
University of Ottawa, Faculty of Health Sciences
-
MAZURKIEWICZ Lukasz
Department of Coronary Artery and Structural Heart Diseases, Institute of Cardiology
-
SAJ Michal
Laboratory of Molecular Biology, Institute of Cardiology
-
TESSON Frederique
University of Ottawa, Faculty of Health Sciences
-
BILINSKA Zofia
Department of Coronary Artery and Structural Heart Diseases, Institute of Cardiology
-
Saj Michal
Laboratory Of Molecular Biology Institute Of Cardiology
-
Bilinska Zofia
Department Of Coronary Artery And Structural Heart Diseases Institute Of Cardiology
-
Tesson Frederique
University Of Ottawa Faculty Of Health Sciences
-
Mazurkiewicz Lukasz
Department Of Coronary Artery And Structural Heart Diseases Institute Of Cardiology
-
Labib Sarah
University Of Ottawa Faculty Of Health Sciences
関連論文
- Coexisting Polymorphisms of P2Y12 and CYP2C19 Genes as a Risk Factor for Persistent Platelet Activation With Clopidogrel
- Novel keratin 14 hotspot mutation in Dowling-Meara type of epidermolysis bullosa simplex : Strategy to avoid KRT14 pseudogene amplification by a simple approach
- A new c.1621 C>G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis) : genotype-phenotype correlation
- Molecular bases of metachromatic leukodystrophy in Polish patients
- Gene dosage effect of p.Glu170Lys mutation in the KRT5 gene in a Polish family with epidermolysis bullosa simplex