Associated Papers
A newly identified missense mutation in CLCA2 is associated with autosomal dominant cardiac conduction block.
Mao Z et al.
Gene, 2019
[Mutation screening for the causative gene in a four-generation Chinese pedigree with progressive cardiac conduction defect].
Tan XJ et al.
Zhonghua Xin Xue Guan Bing Za Zhi, 2016
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