Condition: Ventricular Fibrillation, Paroxysmal Familial, 1
rs137854604
in
SCN5A
gene and
Ventricular Fibrillation, Paroxysmal Familial, 1
PMID 10940383
2000 We performed genetic screenings of Japanese
IVF
patients and found a novel SCN5A missense mutation (
S1710L
) in one symptomatic
IVF
patient that did
not exhibit
the typical Brugada ECG.