Associated Papers
A Novel NKX2-5 Variant in a Child with Left Ventricular Noncompaction, Atrial Septal Defect, Atrioventricular Conduction Disorder, and Syncope.
Yamada Y et al.
Journal of Clinical Medicine, 2022
An update on genetic variants of the NKX2-5.
Kolomenski JE et al.
Human Mutation, 2020
Association Between Mutations in the NKX2.5 Homeobox, Atrial Septal Defects, Ventricular Noncompaction and Sudden Cardiac Death.
Palomino Doza J et al.
Revista Espanola De Cardiologia (english Ed.), 2018
Clinical and Genetic Diagnosis of Nonischemic Sudden Cardiac Death.
Jiménez-Jáimez J et al.
Revista Espanola De Cardiologia (english Ed.), 2017
Very Long-term Survival Following Resection for Pancreatic Cancer Is Not Explained by Commonly Mutated Genes: Results of Whole-Exome Sequencing Analysis.
Dal Molin M et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2015
25623214 (PubMed )
Supplement: 10780432ccr142600-sup-138373_1_supp_2787887_ng4417.xlsx › Sheet1
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