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Rett syndrome: think outside the (skull) box

Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder characterized by neurodevelopmental regression between 6 and 18 months of life and associated with multi-system comorbidities. Caused mainly by pathogenic variants in the MECP2 (methyl CpG binding protein 2) gene, it is the second...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Fac Rev
Prif Awduron: Borloz, Emilie, Villard, Laurent, Roux, Jean-Christophe
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Faculty Opinions Ltd 2021
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC8265562/
https://ncbi.nlm.nih.gov/pubmed/34308425
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12703/r/10-59
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