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Page 1
Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy.
Eur Heart J. 2021 Aug 21;42(32):3063-3073. doi: 10.1093/eurheartj/ehab424.
Eur Heart J. 2021.
PMID: 34263907
Free PMC article.
Fate of a Naive T Cell: A Stochastic Journey.
de la Higuera L, López-García M, Castro M, Abourashchi N, Lythe G, Molina-París C.
de la Higuera L, et al.
Front Immunol. 2019 Mar 6;10:194. doi: 10.3389/fimmu.2019.00194. eCollection 2019.
Front Immunol. 2019.
PMID: 30894850
Free PMC article.
Review.
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New Insights into Renal Failure in a Cohort of 317 Patients with Autosomal Dominant Forms of Alport Syndrome: Report of Two Novel Heterozygous Mutations in COL4A3.
García-Aznar JM, De la Higuera L, Besada Cerecedo L, Gandiaga NP, Vega AI, Fernández-Fresnedo G, González-Lamuño D.
García-Aznar JM, et al. Among authors: de la higuera l.
J Clin Med. 2022 Aug 19;11(16):4883. doi: 10.3390/jcm11164883.
J Clin Med. 2022.
PMID: 36013122
Free PMC article.
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