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New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy.
J Allergy Clin Immunol. 2018 May;141(5):1924-1927.e18. doi: 10.1016/j.jaci.2017.12.995. Epub 2018 Mar 2.
J Allergy Clin Immunol. 2018.
PMID: 29408330
No abstract available.
Hereditary spastic paraplegia associated with a novel homozygous intronic noncanonical splice site variant in the AP4B1 gene.
Gómez-González C, Pizarro-Sánchez C, Rodríguez-Antolín C, Pascual-Pascual I, Garcia-Romero M, Rodriguez-Jiménez C, de Sancho-Martín R, Del Pozo-Mate Á, Solís-López M, Prior-de Castro C, Torres RJ.
Gómez-González C, et al. Among authors: del pozo mate a.
Ann Hum Genet. 2022 May;86(3):109-118. doi: 10.1111/ahg.12455. Epub 2021 Dec 20.
Ann Hum Genet. 2022.
PMID: 34927723
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Genetics of inborn errors of immunity: Diagnostic strategies and new approaches to CNV detection.
Pérez EM, Torbay AG, López MS, de la Cámara RCM, Jiménez CR, Álvarez MÁM, Blanco JN, Gianelli C, Hijón CC, Granados EL, Pena RR, Del Pozo Mate Á, García-Morato MB.
Pérez EM, et al. Among authors: del pozo mate a.
Eur J Clin Invest. 2024 Jun;54(6):e14191. doi: 10.1111/eci.14191. Epub 2024 Mar 5.
Eur J Clin Invest. 2024.
PMID: 38440843
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Molecular diagnosis of cystic fibrosis by RNA obtained from nasal epithelial cells.
Prior-de Castro C, Martínez Gallego MÁ, Gómez-González C, de Sancho Martín R, Rodríguez-Antolín C, Rodríguez-Jiménez C, Del Pozo Mate Á, Zamarrón de Lucas E, Ruiz de Valbuena Maiz M, de Manuel Gómez C, Alcolea Batres S, Prados Sánchez MC, J Torres R.
Prior-de Castro C, et al. Among authors: del pozo mate a.
J Cyst Fibros. 2024 Jul;23(4):788-795. doi: 10.1016/j.jcf.2023.12.007. Epub 2023 Dec 26.
J Cyst Fibros. 2024.
PMID: 38151412
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