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Advance in Genomics of Rare Genetic Diseases.
Sommariva E, Bellin M, Di Resta C. Sommariva E, et al. Among authors: di resta c. Biomolecules. 2023 Sep 25;13(10):1441. doi: 10.3390/biom13101441. Biomolecules. 2023. PMID: 37892123 Free PMC article.
Editorial: Whole Genome Sequencing for rare diseases.
Di Resta C, D'Argenio V. Di Resta C, et al. Front Med (Lausanne). 2023 Sep 19;10:1267930. doi: 10.3389/fmed.2023.1267930. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37795418 Free PMC article. No abstract available.
Genetic background of mitral valve prolapse.
Guicciardi NA, De Bonis M, Di Resta C, Ascione G, Alfieri O, Maisano F, Vergara P. Guicciardi NA, et al. Among authors: di resta c. Rev Cardiovasc Med. 2022 Mar 12;23(3):96. doi: 10.31083/j.rcm2303096. Rev Cardiovasc Med. 2022. PMID: 35345263 Free article. Review.
Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells.
Salvarani N, Peretto G, Silvia C, Villatore A, Thairi C, Santoni A, Galli C, Carrera P, Sala S, Benedetti S, Di Pasquale E, Di Resta C. Salvarani N, et al. Among authors: di resta c. Int J Mol Sci. 2023 May 31;24(11):9548. doi: 10.3390/ijms24119548. Int J Mol Sci. 2023. PMID: 37298497 Free PMC article.
66 results