Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy

Genetic Testing and Molecular Biomarkers

Volumn 16, Issue 6, 2012, Pages 543-549

  Stallmeyer, Birgit ^a,b   Koopmann, Matthias ^a   Schulze Bahr, Eric ^a,b  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b Interdisziplinäres Zentrum für Klinische Forschung IZKF   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

LAMIN A; LAMIN C;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; DISEASE COURSE; DISEASE SEVERITY; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; HEART MUSCLE CONDUCTION DISTURBANCE; HETEROZYGOTE; HUMAN; HUMAN TISSUE; MISSENSE MUTATION; MUSCULAR DYSTROPHY; NONSENSE MUTATION; NUCLEAR FAMILY; NUCLEOTIDE SEQUENCE; PHENOTYPE;

AMINO ACID SEQUENCE; ANIMALS; ARRHYTHMIAS, CARDIAC; CARDIOMYOPATHY, DILATED; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HETEROZYGOTE; HUMANS; LAMIN TYPE A; MALE; MICE; MOLECULAR SEQUENCE DATA; MUSCULAR DYSTROPHIES; MUTATION; MUTATION, MISSENSE; PHENOTYPE; RATS; SEQUENCE ANALYSIS, DNA;

EID: 84862985629     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2011.0214     Document Type: Article

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