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Publications by Elisa Carniel
Whole Exome Sequencing Identifies a Troponin T Mutation Hot Spot in Familial Dilated Cardiomyopathy
PLoS ONE
Multidisciplinary
Prevalence of Desmin Mutations in Dilated Cardiomyopathy
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Related publications
Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Whole Exome Sequencing Identifies a Novel Dominant Missense Mutation Underlying Leukonychia in a Pakistani Family
Journal of Human Genetics
Genetics
Whole-Exome Sequencing Identifies a Potential TTN Mutation in a Multiplex Family With Inguinal Hernia
Hernia : the journal of hernias and abdominal wall surgery
Surgery
Cardiac Troponin T Mutation in Familial Cardiomyopathy With Variable Remodeling and Restrictive Physiology
Clinical Genetics
Genetics
Identification of a Mutation Causing Hypertrophic Cardiomyopathy Using Whole Exome Sequencing: A Proof-Of-Concept
Journal of Cardiology
Cardiovascular Medicine
Cardiology
Familial Dilated Cardiomyopathy
Functional Analysis of a Unique Troponin C Mutation, GLY159ASP, That Causes Familial Dilated Cardiomyopathy, Studied in Explanted Heart Muscle
Circulation. Heart failure
Medicine
Cardiovascular Medicine
Cardiology
Familial Dilated Cardiomyopathy
JAAPA : official journal of the American Academy of Physician Assistants
Nurse Assisting
Familial Dilated Cardiomyopathy
