Discover open access scientific publications

Search, annotate, share and cite publications

Publications by D. W. Benson

A Mouse Model of Human Congenital Heart Disease: High Incidence of Diverse Cardiac Anomalies and Ventricular Noncompaction Produced by Heterozygous Nkx2-5 Homeodomain Missense Mutation

Circulation: Cardiovascular Genetics
2014English

Related publications

Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2011English

Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure

Journal of Clinical Medicine
2020English

TRPM4 Mutation in Patients With Ventricular Noncompaction and Cardiac Conduction Disease

Circulation. Genomic and precision medicine
GeneticsCardiovascular MedicineCardiology
2018English

Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

Heart
Cardiovascular MedicineCardiology
2011English

Complex Trait Analysis of Ventricular Septal Defects Caused by Nkx2-5 Mutation

Circulation: Cardiovascular Genetics
2012English

Somatic NKX2-5 Mutations as a Novel Mechanism of Disease in Complex Congenital Heart Disease

Journal of Medical Genetics
Genetics
2004English

Nkx2-5 Mutation Causes Anatomic Hypoplasia of the Cardiac Conduction System

Journal of Clinical Investigation
Medicine
2004English

Unconventional 2:1 Ventricular Pacing in a Neonate With Congenital Heart Block and Biventricular Noncompaction

Texas Heart Institute Journal
MedicineCardiovascular MedicineCardiology
2019English

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

BioMed Research International
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy