Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype.

Name: Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype.
Author: Maruthappu, T

Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype. — المؤلف: Maruthappu, T — The British journal of dermatology 20200731

المؤلف: Maruthappu, T
النشر: The British journal of dermatology 20200731
الوصف: 1114-1122 p.
الموضوعات: Adolescent؛ Adult؛ Aged؛ Aged, 80 and over؛ Cardiomyopathies؛ Cardiomyopathy, Dilated؛ DNA Mutational Analysis؛ Desmoplakins