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Article

Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families.

Journal of electrocardiology - 1 Jan 2000

Zafari Zahra, Dalili Mohammad, Zeinali Sirus, Saber Siamak, Fazeli Far Amir Farjam, Akbari Mohammad Taghi

Abstract excerpt

BACKGROUND: One of the foremost causes of sudden cardiac death in the young is an inherent cardiac arrhythmia known as Long-QT syndrome (LQTS). Whereas heterozygous mutations typically lead to the Romano-Ward type of LQTS, We have provided a further evidence for the recessive transmission of a novel KCNQ1 gene mutation in two consanguineous families for the first time in Iran. METHODS: Next generation sequencing,...

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Source

Identifiers

PMID: 29033053
DOI: 10.1016/j.jelectrocard.2017.07.012

Genes

KCNQ1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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