Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Maria Qureshi

1PUBLICATIONS
11CO-AUTHORS
Cardiology (incl. cardiovascular diseases)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (1)

Sort by Publication Date:
|Jun 14, 2022
Loss-of-Function <i>FLNC</i> Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population.

Eric D Carruth, Maria Qureshi, Amro Alsaid

Pageof 1

Frequent Collaborators

1 joint publications

Eric D Carruth

1 joint publications

Amro Alsaid

1 joint publications

Melissa A Kelly

1 joint publications

Hugh Calkins

1 joint publications

Brittney Murray

1 joint publications

Amy C Sturm

1 joint publications

Aris Baras

1 joint publications

H Lester Kirchner

1 joint publications

Brandon K Fornwalt

1 joint publications

Cynthia A James

Frequent Collaborators

1 joint publications

Eric D Carruth

1 joint publications

Amro Alsaid

1 joint publications

Melissa A Kelly

1 joint publications

Hugh Calkins

Top Related Videos

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on : Aug 08, 2022

3.7K
See more related videos

Top Related Videos

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on : Aug 08, 2022

3.7K
See more related videos