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Isolated X-linked hypertrophic cardiomyopathy caused by a novel mutation of the four-and-a-half LIM domain 1 gene.

Authors
  • Hartmannova, Hana
  • Kubanek, Milos
  • Sramko, Marek
  • Piherova, Lenka
  • Noskova, Lenka
  • Hodanova, Katerina
  • Stranecky, Viktor
  • Pristoupilova, Anna
  • Sovova, Jana
  • Marek, Tomas
  • Maluskova, Jana
  • Ridzon, Petr
  • Kautzner, Josef
  • Hulkova, Helena
  • Kmoch, Stanislav
Type
Published Article
Journal
Circulation Cardiovascular Genetics
Publisher
Ovid Technologies Wolters Kluwer -American Heart Association
Publication Date
Dec 01, 2013
Volume
6
Issue
6
Pages
543–551
Identifiers
DOI: 10.1161/CIRCGENETICS.113.000245
PMID: 24114807
Source
Medline
Keywords
License
Unknown

Abstract

We identified a novel FHL1 mutation causing isolated hypertrophic cardiomyopathy with X-chromosomal inheritance.

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