Jervell And Lange-nielsen Syndrome 2
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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- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 08, 2023
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