TY  - GEN
AU  - Maruthappu,T
AU  - Posafalvi,A
AU  - Castelletti,S
AU  - Delaney,P J
AU  - Syrris,P
AU  - O'Toole,E A
AU  - Green,K J
AU  - Elliott,P M
AU  - Lambiase,P D
AU  - Tinker,A
AU  - McKenna,W J
AU  - Kelsell,D P
TI  - Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype
SN  - 1365-2133
PY  - 2020///0731
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Cardiomyopathies
KW  - diagnosis
KW  - Cardiomyopathy, Dilated
KW  - DNA Mutational Analysis
KW  - Desmoplakins
KW  - genetics
KW  - Female
KW  - Hair Diseases
KW  - Heart
KW  - diagnostic imaging
KW  - Heterozygote
KW  - Humans
KW  - Keratoderma, Palmoplantar
KW  - Loss of Function Mutation
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Middle Aged
KW  - Pedigree
KW  - Protein Isoforms
KW  - Skin
KW  - pathology
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1111/bjd.17388
ER  -