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资源简介：
A familial disorder of altered DNA-methylation
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创建时间：
2014-07-01
相关数据集
New COLEC10 mutations found in families MC19 and MC25
New COLEC10 mutations found in families MC19 and MC25
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Additional file 2 of Positive renal familial history in IgA nephropathy is associated with worse renal outcomes: a single-center longitudinal study
Additional file 2. Summary of studies reporting clinical features and renal prognosis of familial IgA nephropathy.
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Supplementary Material for: Familial kidney disease phenocopying hypertensive nephropathy
Introduction Familial kidney disease is common in Cyprus and previous studies have found that the majority of families have mutations in Alport syndrome genes COL4A3/4/5. We have collected data from o
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Genetic analysis and family screening for dilated cardiomyopathy: a retrospective analysis of the stepwise pedigree approach
This study aimed to assess the practicality of using a stepwise pedigree-based approach to differentiate between familial and sporadic Dilated Cardiomyopathy (DCM), while also considering timing of th
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Data_Sheet_1_Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report.PDF
BackgroundLeft ventricular non-compaction (LVNC) is an abnormality of the myocardium, characterized by prominent left ventricular trabeculae and deep inter-trabecular recesses. Long QT syndrome (LQTS)
NIAID Data Ecosystem50
