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Publications by L. Pradhan

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

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Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

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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
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2018English

Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

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

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

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2004English

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

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

Texas Heart Institute Journal
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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

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