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43. A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy. Goel N; Huddleston CB; Fiore AC Turk J Pediatr; 2018; 60(3):315-318. PubMed ID: 30511546 [TBL] [Abstract][Full Text] [Related]
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58. Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers. Verdonschot JAJ; Robinson EL; James KN; Mohamed MW; Claes GRF; Casas K; Vanhoutte EK; Hazebroek MR; Kringlen G; Pasierb MM; van den Wijngaard A; Glatz JFC; Heymans SRB; Krapels IPC; Nahas S; Brunner HG; Szklarczyk R Mol Genet Genomic Med; 2020 Feb; 8(2):e1049. PubMed ID: 31880413 [TBL] [Abstract][Full Text] [Related]
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