From: Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation
Individuals
DTNA(NM_001198943.1) (c.G681C)
NEBL(NM_006393.3) (c.T298C)
SCN5A(NM_001099404.2) (c.A1673G)
III-1
GC
TT
AG
III-3
GG
III-5
TC
IV-2
IV-3
IV-4
IV-5