Listar Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 por autor "ADER, Flavie"
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Abnormal Cellular Phenotypes Induced by Three /LAP2 Variants Identified in Men with Cardiomyopathies.
(Cells. vol. 12, n° 2, pp. 337, 2023-01-16)Article de revueLibre acceso
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NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.
(Circulation: Genomic and Precision Medicine. vol. 17, n° 1, pp. e004285, 2024-02-01)Article de revue