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New KCNQ1 c.604+1G>C variant associated with Jervell-Lange Nielsen syndrome in homozygosity and compound heterozygosity.

Revista espanola de cardiologia (English ed.) - 1 Jun 2022

Arana-Rueda Eduardo, Pezzotti Maria-Rosa, Pedrote Alonso, Marcos-Fuentes Laura, Frutos-López Manuel, Castellano Antonio

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PMID: 35144896
DOI: 10.1016/j.rec.2021.11.019

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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New KCNQ1 c.604+1G>C variant associated with Jervell-Lange Nielsen syndrome in homozygosity and compound heterozygosity.PMID 35144896Read ↗

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