Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation-Reference-Cited by-同舟云学术

Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation

Published:2018-02-20 Issue:4 Volume:7 Page:
ISSN:2047-9980
Container-title:Journal of the American Heart Association
language:en
Short-container-title:JAHA

Author:

Frustaci Andrea¹²,De Luca Alessandro³,Guida Valentina³,Biagini Tommaso⁴,Mazza Tommaso⁴,Gaudio Carlo¹,Letizia Claudio⁵,Russo Matteo Antonio⁶,Galea Nicola⁷,Chimenti Cristina¹²

Affiliation:

1. Department of Cardiovascular, Respiratory, Nephrologic, Anesthesiologic and GeriatricSciences, Sapienza University, Rome, Italy

2. Cellular and Molecular Lab, IRCCS L. Spallanzani, Rome, Italy

3. Molecular Genetics Unit, Casa Sollievo della Sofferenza Hospital, IRCCS, San Giovanni Rotondo, Italy

4. Bioinformatics Unit, Casa Sollievo della Sofferenza Hospital, IRCCS, San Giovanni Rotondo, Italy

5. Department of Internal Medicine, Center for Secondary Hypertension, Sapienza University, Rome, Italy

6. IRCCS San Raffaele Pisana, and MEBIC Consortium, San Raffaele Rome Open University, Rome, Italy

7. Department of Radiological, Oncological and Pathological Sciences, La Sapienza University, Rome, Italy

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference29 articles.

1. Contemporary Definitions and Classification of the Cardiomyopathies

2. Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy

3. Recent advancements in the molecular genetics of left ventricular noncompaction cardiomyopathy

4. Left ventricular non-compaction cardiomyopathy

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