A very long-term observation of a family with dilated cardiomyopathy and overlapping phenotype from lamin A/C mutation-Reference-Cited by-同舟云学术

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A very long-term observation of a family with dilated cardiomyopathy and overlapping phenotype from lamin A/C mutation

Published:2020-07-18 Issue:1 Volume:22 Page:53-58
ISSN:1558-2027
Container-title:Journal of Cardiovascular Medicine
language:en
Short-container-title:

Author:

Porcu Maurizio,Corda Marco,Pasqualucci Daniele,Binaghi Giulio,Sanna Nadia,Matta Gildo,Cossa Stefano,Scalone Antonio,Tola Gianfranco

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference27 articles.

1. A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1;Kass;Nat Genet,1994

2. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N Engl J Med,1999

3. Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy;van der Kooi;Neurology,2002

4. Phenotypic diversity in patients with lipodystrophy associated with LMNA mutations;Mory;Eur J Endocrin,2012

5. Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy;Benedetti;J Neurol Neurosurg Psychiatry,2005

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Updates in heart failure: sodium glucose co-transporter 2 inhibitors and beyond – major changes are coming;Journal of Cardiovascular Medicine;2022-12

2. Effects of mutant lamins on nucleo-cytoskeletal coupling in Drosophila models of LMNA muscular dystrophy;Frontiers in Cell and Developmental Biology;2022-08-31

3. Regulation of Lipid Metabolism by Lamin in Mutation-Related Diseases;Frontiers in Pharmacology;2022-02-25

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