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Rett Syndrome (RTT) is a rare X-linked neurodevelopmental disorder, mainly caused by mutations in the MECP2 gene. Reduction in monoamine levels in RTT patients and mouse models suggested the possibility to rescue clinical phenotypes through antidepre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de9f1ecd538f7ca5638961af2644b423
https://doi.org/10.1101/2021.12.17.473107
https://doi.org/10.1101/2021.12.17.473107
Publikováno v:
Experimental neurology. 353
Rett Syndrome (RTT) is a rare X-linked neurodevelopmental disorder, mainly caused by mutations in the MECP2 gene. Reduction in monoamine levels in RTT patients and mouse models suggested the possibility to rescue clinical phenotypes through antidepre