A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.

Abstract excerpt

Cardiac conduction defects that are associated with dilated cardiomyopathy (DCM) are generally considered to be sporadic clinical entities, although familial forms of disorders with these clinical features have been identified in a number of families in different countries. An autosomal dominant cardiac disorder characterised by conduction abnormalities and DCM, termed progressive familial heart block type II...

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