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Gabrielle Wright

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Busse L, Huth E, Abraham M, Abraham T, Padmanabhan A, Wojciak J, et al.
medRxiv . 2024 Nov; PMID: 39606411
Hypertrophic cardiomyopathy (HCM) is a genetically heterogeneous disorder with several established genotype-phenotype relationships. While biallelic truncating variants in the gene cause severe congenital HCM, recent studies have associated heterozygous truncating...