Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Jervell-Lange Nielsen Syndrome and KCNQ1[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 |
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