Protein Molecular Modeling Techniques Investigating Novel TAB2 Variant R347X Causing Cardiomyopathy and Congenital Heart Defects in Multigenerational Family

Molecular genetics & genomic medicine- United States

doi 10.1002/mgg3.401

Full Text

Abstract

Available in

Date

Authors

Publisher

Wiley

Related search

Imaging Techniques for Visualizing and Phenotyping Congenital Heart Defects in Murine Models

Birth Defects Research Part C - Embryo Today: Reviews
MedicineEmbryologyDevelopmental Biology
2013English

A Systematic Variant Screening in Familial Cases of Congenital Heart Defects Demonstrates the Usefulness of Molecular Genetics in This Field

European Journal of Human Genetics
Genetics
2015English

Copy Number Variation in Congenital Heart Defects

Current Genetic Medicine Reports
2014Dutch

Recurrence of Congenital Heart Defects in Families

Circulation
Cardiovascular MedicinePhysiologyCardiology
2009English

Comprehensive Approach to Congenital Heart Defects

Journal of Cardiovascular Disease Research
Cardiovascular MedicineCardiology
2017English

Congenital Anomalies in the Heart With Hypertrophic Cardiomyopathy.

Heart
Cardiovascular MedicineCardiology
1968English

A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family With Dilated Cardiomyopathy (FDCM)

PLoS ONE
Multidisciplinary
2014English

MESP1 Mutations in Patients With Congenital Heart Defects

Human Mutation
Genetics
2016English

Extracardiac Defects in Children With Congenital Heart Disease.

Heart
Cardiovascular MedicineCardiology
1979English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy