Browsing Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 by Author "MAITZ, Silvia"
Now showing items 1-2 of 2
-
De novo variants in ATP2B1 lead to neurodevelopmental delay.
RAHIMI, Meer Jacob; URBAN, Nicole; WEGLER, Meret ...(American Journal of Human Genetics. vol. 109, n° 5, pp. 944-952, 2022-05-05)Article de revueOpen access -
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for -Related Syndrome.
FOROUTAN, Aidin; HAGHSHENAS, Sadegheh; BHAI, Pratibha ...(International Journal of Molecular Sciences. vol. 23, n° 3, 2022-02-05)Article de revueOpen access