Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Jervell Lange-nielsen Syndrome[original query] |
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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. Hereditas 2017 12 154 16. Olsson K Sigvard, Wålinder Olof, Jansson Ulf, Wilbe Maria, Bondeson Marie-Louise, Stattin Eva-Lena, Raha-Chowdhury Ruma, Williams Rog |
Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families. Journal of arrhythmia 2018 6 34 (3): 286-290. Amirian Azam, Zafari Zahra, Dalili Mohammad, Saber Siamak, Karimipoor Morteza, Dabbagh Bagheri Samira, Fazelifar Amir Farjam, Zeinali Siro |
Left cardiac sympathetic denervation in children with Jervell Lange-Nielsen syndrome and drug refractory torsades - A case series. Pacing and clinical electrophysiology : PACE 2023 9 . Deepanjan Bhattacharya, Narayanan Namboodiri, Madhusoodanan Pillai Sreelekshmi, Mukund A Prabhu, Abhilash Sreevilasam Pushpangadhan, Sabarinath Menon, Baiju S Dharan, Ajitkumar Valaparamb |
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- Page last updated:May 13, 2024
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