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Genetics of cardiomyopathies: novel perspectives with next generation sequencing.
Monserrat L, Ortiz-Genga M, Lesende I, Garcia-Giustiniani D, Barriales-Villa R, de Una-Iglesias D, Syrris P, Castro-Beiras A. Monserrat L, et al. Among authors: de una iglesias d. Curr Pharm Des. 2015;21(4):418-30. doi: 10.2174/138161282104141204123748. Curr Pharm Des. 2015. PMID: 25483943 Review.
Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy.
Ochoa JP, Lopes LR, Perez-Barbeito M, Cazón-Varela L, de la Torre-Carpente MM, Sonicheva-Paterson N, De Uña-Iglesias D, Quinn E, Kuzmina-Krutetskaya S, Garrote JA, Elliott PM, Monserrat L. Ochoa JP, et al. Among authors: de una iglesias d. Clin Genet. 2020 Jul;98(1):86-90. doi: 10.1111/cge.13759. Epub 2020 May 11. Clin Genet. 2020. PMID: 32335906
Identification by next-generation sequencing of 2 novel cases of noncompaction cardiomyopathy associated with 1p36 deletions.
Peña-Peña ML, Trujillo-Quintero JP, García-Medina D, Cantero-Pérez EM, De Uña-Iglesias D, Monserrat L. Peña-Peña ML, et al. Among authors: de una iglesias d. Rev Esp Cardiol (Engl Ed). 2020 Sep;73(9):780-782. doi: 10.1016/j.rec.2020.02.004. Epub 2020 Mar 16. Rev Esp Cardiol (Engl Ed). 2020. PMID: 32192878 English, Spanish. No abstract available.