Cardiovascular Problems in the Fragile X Premutation.

FMR1 arrhythmia autonomic dysfunction cardiovascular fragile X hypertension premutation

Journal

Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621

Informations de publication

Date de publication:
2020
Historique:
received: 24 07 2020
accepted: 21 09 2020
entrez: 2 11 2020
pubmed: 3 11 2020
medline: 3 11 2020
Statut: epublish

Résumé

There is a dearth of information about cardiovascular problems in fragile X premutation carriers who have 55-200 CGG repeats in fragile X mental retardation 1 (

Identifiants

pubmed: 33133171
doi: 10.3389/fgene.2020.586910
pmc: PMC7578382
doi:

Types de publication

Journal Article

Langues

eng

Pagination

586910

Subventions

Organisme : NICHD NIH HHS
ID : P50 HD103526
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD036071
Pays : United States
Organisme : NICHD NIH HHS
ID : U54 HD079125
Pays : United States

Informations de copyright

Copyright © 2020 Tassanakijpanich, Cohen, Cohen, Srivatsa and Hagerman.

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Auteurs

Nattaporn Tassanakijpanich (N)

UC Davis MIND Institute, UC Davis Health, Sacramento, CA, United States.
Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.

Jonathan Cohen (J)

Fragile X Alliance Clinic, Genetic Clinics Australia, Melbourne, VIC, Australia.

Rashelle Cohen (R)

Fragile X Alliance Clinic, Genetic Clinics Australia, Melbourne, VIC, Australia.

Uma N Srivatsa (UN)

Division of Cardiovascular Medicine, Department of Internal Medicine, UC Davis Medical Center, Sacramento, CA, United States.

Randi J Hagerman (RJ)

UC Davis MIND Institute, UC Davis Health, Sacramento, CA, United States.
Department of Pediatrics, University of California, Davis, Davis, School of Medicine, Sacramento, CA, United States.

Classifications MeSH