Listar Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 por autor "RICHARD, Emmanuel"
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Infantile primary carnitine deficiency: A severe cardiac presentation unresponsive to carnitine supplementation.
LEBRETON, Louis; GASCHIGNARD, Margaux; GUIBET, Claire ...(JIMD reports. vol. 64, n° 1, pp. 35-41, 2023-01-01)Article de revueLibre acceso -
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
BOUTIN, Julian; ROSIER, Juliette; CAPPELLEN, David ...(Nature Communications. vol. 12, n° 1, 2021-08-13)Article de revueLibre acceso