Jervell And Lange-nielsen Syndrome 2
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Last Posted: Sep 28, 2023
- Left cardiac sympathetic denervation in children with Jervell Lange-Nielsen syndrome and drug refractory torsades - A case series.
Deepanjan Bhattacharya, et al. Pacing and clinical electrophysiology : PACE 2023 0 - Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.
Bdier Amnah Y, et al. Molecular genetics & genomic medicine 2017 0 (5) 592-601 - Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.
Olsson K Sigvard, et al. Hereditas 2017 0 16 - Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families.
Amirian Azam, et al. Journal of arrhythmia 2018 0 (3) 286-290 - Comprehensive analysis of syndromic hearing loss patients in Japan.
Ideura Michie, et al. Scientific reports 2019 0 (1) 11976 - 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 - An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition.
Roberts Jason D, et al. Circulation 2020 0 (6) 429-439 - Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome.
Vojdani Samaneh, et al. Fetal and pediatric pathology 2019 4 1-9 - Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children.
Boudewyns An, et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2018 7 (6) 732-738 - KCNQ1 mutations associated with Jervell and Lange-Nielsen syndrome and autosomal recessive Romano-Ward syndrome in India-expanding the spectrum of long QT syndrome type 1.
Vyas Bijal, et al. American journal of medical genetics. Part A 2016 4
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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:Oct 1, 2023
- Page last updated:Dec 08, 2023
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