Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block

Table 1

Demographic and clinic features in members of the family.

Family members	Sex	Age (year)	EGC	History	Mutation
Proband (III-1)	Female	10	High-grade AVB	Syncope	c.2455C>T
II-1	Female	35	—	—	—
II-2	Male	40	PR interval delayed	Syncope	c.2455C>T
II-3	Female	37	—	—	—
I-1	Female	34	—	Sudden death	—
I-2	Male	66	—	—	—

Age of death.