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Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group.

Mestroni, L and Rocco, C and Gregori, D and Sinagra, G and Di Lenarda, A and Miocic, S and Vatta, M and Pinamonti, B and Muntoni, F and Caforio, AL and McKenna, WJ and Falaschi, A and Giacca, M and Camerini, (1999) Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group. J Am Coll Cardiol , 34 (1) 181 - 190.

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Abstract

This study was performed to evaluate the characteristics, mode of inheritance and etiology of familial dilated cardiomyopathy (FDC).

Type:Article
Title:Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group.
Location:UNITED STATES
Language:English
Keywords:Adolescent, Adult, Aged, Aged, 80 and over, Cardiomyopathy, Dilated, Child, Child, Preschool, DNA Mutational Analysis, Dystrophin, Endocardium, Genetic Heterogeneity, Genetic Linkage, Humans, Middle Aged, Muscle, Skeletal, Myocardium, Pedigree, Phenotype, Prospective Studies
UCL classification:UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Child Health > Department of Neurosciences and Mental Health > ICH - Dubowitz Neuromuscular Centre

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