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Article

RettDb: the Rett syndrome omics database to navigate the Rett syndrome genomic landscape.

Database : the journal of biological databases and curation - 16 Oct 2024

Cillari Nico, Neri Giuseppe, Pisanti Nadia, Milazzo Paolo, Borello Ugo

Abstract excerpt

Rett syndrome (RTT) is a neurodevelopmental disorder occurring almost exclusively in females and leading to a variety of impairments and disabilities from mild to severe. In >95% cases, RTT is due to mutations in the X-linked gene MECP2, but the molecular mechanisms determining RTT are unknown at present, and the complexity of the system is challenging. To facilitate and provide guidance to the unraveling of...

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Identifiers

PMID: 39414258
DOI: 10.1093/database/baae109
PMCID: PMC11482253

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