Literature DB >> 23424253

Assigning a causal role to genetic variants in hypertrophic cardiomyopathy.

Hugh Watkins.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2013        PMID： 23424253     DOI： 10.1161/CIRCGENETICS.111.000032

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN： 1942-3268


× No keyword cloud information.
  4 in total

1.  Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.

Authors:  Chloe Reuter; Megan E Grove; Kate Orland; Katherine Spoonamore; Colleen Caleshu
Journal:  J Genet Couns       Date:  2017-12-12       Impact factor: 2.537

Review 2.  Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy.

Authors:  Catarina Roma-Rodrigues; Alexandra R Fernandes
Journal:  Appl Clin Genet       Date:  2014-10-03

Review 3.  Recent advances in hypertrophic cardiomyopathy.

Authors:  Teerapat Yingchoncharoen; Wh Wilson Tang
Journal:  F1000Prime Rep       Date:  2014-02-03

4.  Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction.

Authors:  Robert Hastings; Carin P de Villiers; Charlotte Hooper; Liz Ormondroyd; Alistair Pagnamenta; Stefano Lise; Silvia Salatino; Samantha J L Knight; Jenny C Taylor; Kate L Thomson; Linda Arnold; Spyros D Chatziefthimiou; Petr V Konarev; Matthias Wilmanns; Elisabeth Ehler; Andrea Ghisleni; Mathias Gautel; Edward Blair; Hugh Watkins; Katja Gehmlich
Journal:  Circ Cardiovasc Genet       Date:  2016-09-13
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.