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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 - 3 (of 3 Records)

Query Trace: Counseling and LMNA[original query]
Genetic basis of hypertrophic cardiomyopathy in children.
Clinical research in cardiology : official journal of the German Cardiac Society 2018 Aug .
Rupp Stefan, Felimban Moataz, Schänzer Anne, Schranz Dietmar, Marschall Christoph, Zenker Martin, Logeswaran Thushiha, Neuhäuser Christoph, Thul Josef, Jux Christian, Hahn Andre
Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report.
Molecular medicine reports 2020 Apr .
Fan Peng, Zhang Di, Yang Kun-Qi, Tian Tao, Luo Fang, Liu Ya-Xin, Wang Lin-Ping, Zhou Xian-Lia
Two Moroccan Families with Emery-Dreifuss Muscular Dystrophy and Report of a Novel LMNA Pathogenic Variant.
Molecular syndromology 2024 12 15 (6): 517-522.
Yasmina Rahmuni, Youssef El Kadiri, Jaber Lyahyai, Nezha Birouk, Mounir Nesnassi, Abdelaziz Sefiani, Ilham Rat
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