Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype
出版年份 2018 全文链接
标题
Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype
作者
关键词
-
出版物
BRITISH JOURNAL OF DERMATOLOGY
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2018-11-01
DOI
10.1111/bjd.17388
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation
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- Truncating Plakophilin-2 Mutations in Arrhythmogenic Cardiomyopathy Are Associated With Protein Haploinsufficiency in Both Myocardium and Epidermis
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- (2011) Jamie D. Kapplinger et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: Proposed Modification of the Task Force Criteria
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- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
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