Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Ebstein's Anomaly[original query] |
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NKX2.5 mutations in patients with non-syndromic congenital heart disease. International journal of cardiology 2010 Feb 138 (3): 261-5. Gioli-Pereira Luciana, Pereira Alexandre Costa, Mesquita Sônia M, Xavier-Neto José, Lopes Antônio Augusto, Krieger José Eduar |
Rare loss-of-function variants in matrisome genes are enriched in Ebstein's anomaly. HGG advances 2023 11 100258. Zhou Zhou, Xia Tang, Wen Chen, Qianlong Chen, Bo Ye, Angad S Johar, Iftikhar J Kullo, Keyue Di |
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