Calmodulin, sudden death, and the Folbigg case: genes in court-Reference-Cited by-同舟云学术

Calmodulin, sudden death, and the Folbigg case: genes in court

Published:2024-04-09 Issue:20 Volume:45 Page:1801-1803
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:

Author:

Schwartz Peter J¹^ORCID,Crotti Lia¹²^ORCID,Nyegaard Mette³⁴^ORCID,Overgaard Michael Toft⁵^ORCID

Affiliation:

1. Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Istituto Auxologico Italiano, IRCCS , Via Pier Lombardo, 22, Milano 20135 , Italy

2. Department of Medicine and Surgery, University of Milano-Bicocca , Milano , Italy

3. Department of Congenital Disorders, Statens Serum Institute , Copenhagen , Denmark

4. Department of Health Science and Technology, Aalborg University , Aalborg , Denmark

5. Department of Chemistry and Bioscience, Aalborg University , Aalborg , Denmark

Funder

Bibliosan

Novo Nordisk

Publisher

Oxford University Press (OUP)

Link

https://academic.oup.com/eurheartj/article-pdf/45/20/1801/57927970/ehae152.pdf

Reference16 articles.

1. She was convicted of killing her four children. Could a gene mutation set her free?;Phillips;Nature,2022

2. ‘Science was heard’: woman who was convicted of killing her children pardoned after inquiry;Lewis;Nature,2023

3. The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy;Schwartz;Eur Heart J,2013

4. Inherited cardiac arrhythmias;Schwartz;Nat Rev Dis Primers,2020

5. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy;Schwartz;Circulation,1995

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