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Publications by Pierluigi Aragona

Whole Exome Sequencing Identifies a Troponin T Mutation Hot Spot in Familial Dilated Cardiomyopathy

Multidisciplinary

English

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Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease

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Whole Exome Sequencing Identifies a Novel Dominant Missense Mutation Underlying Leukonychia in a Pakistani Family

Journal of Human Genetics

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Whole-Exome Sequencing Identifies a Potential TTN Mutation in a Multiplex Family With Inguinal Hernia

Hernia : the journal of hernias and abdominal wall surgery

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Cardiac Troponin T Mutation in Familial Cardiomyopathy With Variable Remodeling and Restrictive Physiology

Clinical Genetics

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Identification of a Mutation Causing Hypertrophic Cardiomyopathy Using Whole Exome Sequencing: A Proof-Of-Concept

Journal of Cardiology

Cardiovascular Medicine

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Familial Dilated Cardiomyopathy

English

Functional Analysis of a Unique Troponin C Mutation, GLY159ASP, That Causes Familial Dilated Cardiomyopathy, Studied in Explanted Heart Muscle

Circulation. Heart failure

Cardiovascular Medicine

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Familial Dilated Cardiomyopathy

JAAPA : official journal of the American Academy of Physician Assistants

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Familial Dilated Cardiomyopathy

English