Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
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Records 1 - 7 (of 7 Records) |
| Query Trace: Wolff-parkinson-white Syndrome[original query] |
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| The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White. European journal of human genetics : EJHG 2007 Feb 15 (2): 155-61. Ruiter E Mariken, Siers Marloes H, van den Elzen Christa, van Engelen Baziel G, Smeitink Jan A M, Rodenburg Richard J, Hol Frans |
| High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation. Neurology 2013 Jan 80 (1): 100-5. Malfatti Edoardo, Laforêt Pascal, Jardel Claude, Stojkovic Tanya, Behin Anthony, Eymard Bruno, Lombès Anne, Benmalek Amria, Bécane Henri-Marc, Berber Nawal, Meune Christophe, Duboc Denis, Wahbi Kar |
| Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus. American journal of medical genetics. Part A 2015 Aug . Bowles Neil E, Jou Chuanchau J, Arrington Cammon B, Kennedy Brett J, Earl Aubree, Matsunami Norisada, Meyers Lindsay L, Etheridge Susan P, Saarel Elizabeth V, Bleyl Steven B, Yost H Joseph, Yandell Mark, Leppert Mark F, Tristani-Firouzi Martin, Gruber Peter J, |
| A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations. BMC medical genetics 2015 16 21. Truszkowska Gra?yna T, Bili?ska Zofia T, Kosi?ska Joanna, ?leszycka Justyna, Rydzanicz Ma?gorzata, Sobieszcza?ska-Ma?ek Ma?gorzata, Franaszczyk Maria, Bili?ska Maria, Stawi?ski Piotr, Michalak Ewa, Ma?ek ?ukasz A, Chmielewski Przemys?aw, Foss-Nieradko Bogna, Machnicki Marcin M, Stok?osa Tomasz, Poni?ska Joanna, Szumowski ?ukasz, Grzybowski Jacek, Piwo?ski Jerzy, Drygas Wojciech, Zieli?ski Tomasz, P?oski Raf |
| PRKAG3 polymorphisms associated with sporadic Wolff-Parkinson-White syndrome among a Taiwanese population. Journal of the Chinese Medical Association : JCMA 2016 Dec 79 (12): 656-660. Weng Ken-Pen, Yuh Yeong-Seng, Huang Shih-Hui, Hsiao Hsiang-Chiang, Wu Huang-Wei, Chien Jen-Hung, Chen Bo-Hau, Huang Shih-Ming, Chien Kuang-Jen, Ger Luo-Pi |
| Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399. Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema |
| Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population. Medicine 2022 Aug 101 (32): e30046. Han Bing, Wang Yongxiang, Zhao Jing, Lan Qingsu, Zhang Jin, Meng Xiaoxue, Jin Jianjian, Bai Ming, Zhang Zhe |
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