Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano–Ward Syndrome: Functional Characterization by Mutant Co-expression

Next Generation Sequencing has identified many KCNQ1 genetic variants associated with type 1 long QT or Romano-Ward syndrome, most frequently inherited in an autosomal dominant fashion, although recessive forms have been reported. Particularly in the case of missense variants, functional studies of...

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Detalles Bibliográficos
Autores principales: González-Garrido, Antonia, Domínguez-Pérez, Mayra, Jacobo-Albavera, Leonor, López-Ramírez, Omar, Guevara-Chávez, José Guadalupe, Zepeda-García, Oscar, Iturralde, Pedro, Carnevale, Alessandra, Villarreal-Molina, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937651/
https://www.ncbi.nlm.nih.gov/pubmed/33693037
http://dx.doi.org/10.3389/fcvm.2021.625449

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937651/
https://www.ncbi.nlm.nih.gov/pubmed/33693037
http://dx.doi.org/10.3389/fcvm.2021.625449

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