Condition: Syncope
rs1554919471 in
KCNQ1 gene and
Syncope
PMID 29372044 2018 Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.
PMID 29033053 2018 Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families.