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ArticleJCI insight2024

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension.

Ian Copeland et al.PubMed ↗Full text ↗Publisher ↗

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3 papers cite it

2024
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2026
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Full record →Abstract, authors, funding and every citing paper · PMID 38716726