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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Hearing Loss and KCNQ1[original query]
The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss.
Human mutation 2006 Aug 27 (8): 786-95.
Van Laer Lut, Carlsson Per-Inge, Ottschytsch Natacha, Bondeson Marie-Louise, Konings Annelies, Vandevelde Ann, Dieltjens Nele, Fransen Erik, Snyders Dirk, Borg Erik, Raes Adam, Van Camp G
Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss.
Annals of human genetics 2009 Jul 73 (Pt 4): 411-21.
Pawelczyk Malgorzata, Van Laer Lut, Fransen Erik, Rajkowska Elzbieta, Konings Annelies, Carlsson Per-Inge, Borg Erik, Van Camp Guy, Sliwinska-Kowalska Mario
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
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
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul .
Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
Journal of neurology 2021 1 268 (6): 2192-2207.
Chakrabarty Sanjiban, Govindaraj Periyasamy, Sankaran Bindu Parayil, Nagappa Madhu, Kabekkodu Shama Prasada, Jayaram Pradyumna, Mallya Sandeep, Deepha Sekar, Ponmalar J N Jessiena, Arivinda Hanumanthapura R, Meena Angamuthu Kanikannan, Jha Rajan Kumar, Sinha Sanjib, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasamy, Satyamoorthy Kapaet
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