Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy.
cardiomyopathy, hypertrophic
death, sudden, cardiac
disease
mutation
risk
Journal
Circulation. Genomic and precision medicine
ISSN: 2574-8300
Titre abrégé: Circ Genom Precis Med
Pays: United States
ID NLM: 101714113
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
pubmed:
5
9
2020
medline:
28
10
2021
entrez:
5
9
2020
Statut:
ppublish
Résumé
Cardiac troponin I ( We sequenced 29 families with hypertrophic cardiomyopathy enriched for pediatric-onset disease and identified 5 families with the All 5 families with The
Sections du résumé
BACKGROUND
Cardiac troponin I (
METHODS
We sequenced 29 families with hypertrophic cardiomyopathy enriched for pediatric-onset disease and identified 5 families with the
RESULTS
All 5 families with
CONCLUSIONS
The
Identifiants
pubmed: 32885985
doi: 10.1161/CIRCGEN.120.002991
pmc: PMC7676616
doi:
Substances chimiques
Troponin I
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
444-452Subventions
Organisme : Wellcome Trust
ID : 107469
Pays : United Kingdom
Organisme : Howard Hughes Medical Institute
Pays : United States
Organisme : Medical Research Council
ID : MC_UP_1102/20
Pays : United Kingdom
Organisme : NIGMS NIH HHS
ID : T32 GM007753
Pays : United States
Organisme : Wellcome Trust
ID : 107469/Z/15/Z
Pays : United Kingdom
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