Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Deafness and KCNQ1[original query] |
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Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome. Frontiers of medicine in China 2007 Jul 1 (3): 312-5. Du Rong, Tian Li, Yuan Guohui, Li Jin, Ren Faxin, Gui Le, Li Wei, Zhang Shouyan, Kang Cailian, Yang Jung |
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. American journal of medical genetics. Part A 2016 Apr . Vyas Bijal, Puri Ratna D, Namboodiri Narayanan, Nair Mohan, Sharma Deepak, Movva Sireesha, Saxena Renu, Bohora Shomu, Aggarwal Neeraj, Vora Amit, Kumar Jatinder, Singh Tarandeep, Verma Ishwar |
Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia. Molecular genetics & genomic medicine 2017 9 5 (5): 592-601. Bdier Amnah Y, Al-Ghamdi Saleh, Verma Prashant K, Dagriri Khalid, Alshehri Bandar, Jiman Omamah A, Ahmed Sherif E, Wilde Arthur A M, Bhuiyan Zahurul A, Al-Aama Jumana |
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 |
Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2018 Jul 39 (6): 732-738. Boudewyns An, van den Ende Jenneke, Sommen Manou, Wuyts Wim, Peeters Nils, Van de Heyning Paul, Van Camp G |
Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome. Fetal and pediatric pathology 2019 Apr 1-9. Vojdani Samaneh, Amirsalari Susan, Milanizadeh Saman, Molaei Fatemeh, Ajalloueyane Mohammad, Khosravi Arezoo, Hamzehzadeh Leila, Ghasemi Mohammad Mehdi, Talee Mohammad Reza, Abbaszadegan Mohammad Re |
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- Page last updated:Mar 29, 2024
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