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Case Report: A Novel NKX2-5 Mutation in a Family With Congenital Heart Defects, Left Ventricular Non-compaction, Conduction Disease, and Sudden Cardiac Death.
Morlanes-Gracia, Paula; Antoniutti, Guido; Alvarez-Rubio, Jorge; Torres-Juan, Laura; Heine-Suñer, Damian; Ripoll-Vera, Tomás.
Affiliation
  • Morlanes-Gracia P; Hospital Clínico Lozano Blesa, Zaragoza, Spain.
  • Antoniutti G; Hospital Universitario Son LLàtzer, Palma de Mallorca, Spain.
  • Alvarez-Rubio J; Hospital Universitario Son LLàtzer, Palma de Mallorca, Spain.
  • Torres-Juan L; Instituto de Investigación Sanitaria Illes Balears (IdISBa), Palma de Mallorca, Spain.
  • Heine-Suñer D; Instituto de Investigación Sanitaria Illes Balears (IdISBa), Palma de Mallorca, Spain.
  • Ripoll-Vera T; Departmento de Genetica Clínica y Molecular, Hospital Universitario Son Espases, Palma de Mallorca, Spain.
Front Cardiovasc Med ; 8: 691203, 2021.
Article in En | MEDLINE | ID: mdl-34277740
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cardiovasc Med Year: 2021 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cardiovasc Med Year: 2021 Document type: Article Affiliation country: Country of publication: