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Table 1 Clinical characteristics of family 186

From: Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families

Pedigree

Genotype

Clinical data

V1

+

CHB, PPM, ASD

V2

+

1st degree AVB

IV.4

+

AVSD, AF

IV.3

+

Normal

IV.5

+

Normal

III.2

NA

PPM

III.3

NA

PPM

II.3

NA

PPM

III.4

NA

SCD

II.6

NA

SCD

III.5

NA

DCM, VT

IV.6

NA

ASD, SCD

III.6

NA

DCM, AF, SCD