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Genetics of cardiomyopathies: novel perspectives with next generation sequencing.
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
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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.
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Development and validation of a next-generation sequencing panel for clinical pharmacogenetics.
Ramudo-Cela L, López-Martí JM, Colmeiro-Echeberría D, De-Uña-Iglesias D, Santomé-Collazo JL, Monserrat-Iglesias L.
Ramudo-Cela L, et al. Among authors: de una iglesias d.
Farm Hosp. 2020 Sep 30;44(6):243-253. doi: 10.7399/fh.11353.
Farm Hosp. 2020.
PMID: 33156743
English.
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