Familial Atrial Fibrillation
What's New
Last Posted: Mar 08, 2023
- A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation.
Mechakra Asma, et al. The American journal of cardiology 2018 0 (5) 787-793 - Putative role of Brugada syndrome genes in familial atrial fibrillation.
Maltese P E, et al. European review for medical and pharmacological sciences 2019 0 (17) 7582-7598 - Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population.
Amirian Azam, et al. Turkish journal of medical sciences 2019 0 (2) 453-457 - ISL1 loss-of-function variation causes familial atrial fibrillation.
Wu Shao-Hui, et al. European journal of medical genetics 2020 0 (11) 104029 - PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.
Guo Xiao-Juan, et al. Journal of the American Heart Association 2021 0 (23) e023517 - KCNQ1 gain-of-function mutation in familial atrial fibrillation.
Chen Yi-Han, et al. Science (New York, N.Y.) 2003 0 (5604) 251-4 - Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
Vad Oliver Bundgaard, et al. Frontiers in genetics 2022 0 806429 - The Genetic Puzzle of Familial Atrial Fibrillation.
Ragab Ahmed A Y et al. Frontiers in cardiovascular medicine 2020 714 - A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
Gudbjartsson Daniel F, et al. European heart journal 2017 0 (1) 27-34 - A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
Wang Jun, et al. European journal of medical genetics 2014 1 (1) 25-31
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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