Wilfredo Gil

Title(s)Clinical Research Coordinator, Medicine
SchoolSchool of Medicine
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    1. Genetic variant affecting the myosin light chain 2 related to familial hypertrophic cardiomyopathy. Intractable Rare Dis Res. 2020 Nov; 9(4):229-232. Gil WS, Ávila Vidal LA, Vásquez Salguero MA, Cajiao MB, Peña CV. PMID: 33139982; PMCID: PMC7586884.
      View in: PubMed   Mentions: 3