Detalhe da pesquisa
1.
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy.
J Mol Cell Cardiol
; 141: 17-29, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32201174
2.
In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.
J Mol Cell Cardiol
; 129: 303-313, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30885746
3.
Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics.
Sci Rep
; 7(1): 13791, 2017 10 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29062102