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Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis

Title:	Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis
Authors:	Palmyre, Aurélien^{Aff1, IDs1302302503815z_cor1}; Koraichi, Fairouz^{Aff1, Aff2}; Ader, Flavie^{Aff3, Aff4, Aff5}; Donal, Erwan^Aff6; Bordet, Céline^Aff2; de Groote, Pascal^{Aff7, Aff8}; Faivre, Laurence^Aff9; Reant, Patricia^Aff10; Toutain, Annick^Aff11; Nguyen, Karine^Aff12; Isidor, Bertrand^Aff13; Brehin, Anne-Claire^Aff14; Legrand, Lise^Aff3; Gandjbakhch, Estelle^{Aff2, Aff3, Aff15}; Proukhnitzky, Julie^{Aff2, Aff3}; Isnard, Richard^Aff15; Mansencal, Nicolas^Aff16; Pruny, Jean-François^Aff2; Rabes, Jean-Pierre^Aff17; Francou, Bruno^Aff18; Caillaud, Catherine^Aff19; Richard, Pascale^{Aff3, Aff4}; Charron, Philippe^{Aff1, Aff2, Aff3, Aff15}
Source:	Orphanet Journal of Rare Diseases. 20(1)
Database:	Springer Nature Journals