Electrical disorders in atrial septal defect: genetics and heritability

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Electrical disorders in atrial septal defect: genetics and heritability

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2018

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Electrical disorders in atrial septal defect: genetics and heritability

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Electrical disorders in atrial septal defect: genetics and heritability

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Electrical disorders in atrial septal defect: genetics and heritability

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Electrical disorders in atrial septal defect: genetics and heritability

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Electrical disorders in atrial septal defect: genetics and heritability

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Electrical disorders in atrial septal defect: genetics and heritability

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P1476

Electrical disorders in atrial septal defect: genetics and heritability

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P2093

Minoru Horie

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P2860

Congenital heart disease caused by mutations in the transcription factor NKX2-5

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

T-box transcription factor Tbx2 represses differentiation and formation of the cardiac chambers

TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome

Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

Gene regulatory networks in cardiac conduction system development

T-box genes in human disorders

Familial heart disease with skeletal malformations

P304

S2848-S2853

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scholarly article

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10.21037/JTD.2018.02.53

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P407

English

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Suppl 24

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P478

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P50

Hisaaki Aoki

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2018-09-01T00:00:00Z

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30305944

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6174139

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