Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 5 (of 5 Records) |
Query Trace: Heart Disorder[original query] |
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Genetic variants in incident SUDEP cases from a community-based prospective cohort with epilepsy. Journal of neurology, neurosurgery, and psychiatry 2019 11 91 (2): 126-131. Ge Yan, Ding Ding, Zhu Guoxing, Kwan Patrick, Wang Wenzhi, Hong Zhen, Sander Josemir |
Identification of a variant hotspot in MYBPC3 and of a novel CSRP3 autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy. Polish archives of internal medicine 2020 Jan . Lipari Martina, Wypasek Ewa, Karpi?ski Marek, Tomkiewicz-Pajak Lidia, Laino Luigi, Binni Francesco, Giannarelli Diana, Rubi? Pawe?, Petkow-Dimitrow Pawe?, Undas Anetta, Grammatico Paola, Bottillo Ire |
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Nature genetics 2021 Jan . Harper Andrew R, Goel Anuj, Grace Christopher, Thomson Kate L, Petersen Steffen E, Xu Xiao, Waring Adam, Ormondroyd Elizabeth, Kramer Christopher M, Ho Carolyn Y, Neubauer Stefan, , Tadros Rafik, Ware James S, Bezzina Connie R, Farrall Martin, Watkins Hu |
A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole?exome sequencing. BMC medical genomics 2022 11 15 (1): 234. Ghasemi Serwa, Mahdavi Mohammad, Maleki Majid, Salahshourifar Iman, Kalayinia Sami |
Somatic GATA4 mutation contributes to tetralogy of Fallot. Experimental and therapeutic medicine 2024 1 27 (2): 91. Pradhan Abhinav, Yan-Jie Li, Ri-Tai Huang, Xing-Yuan Liu, Jia-Ning Gu, Chen-Xi Yang, Ying-Jia Xu, Juan Wang, Yi-Qing Ya |
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