- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-994X
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
MeCP2 mutations: progress towards understanding and treating Rett syndrome ; volume:9 ; number:1 ; day:17 ; month:2 ; year:2017 ; pages:1-4 ; date:12.2017
Genome medicine ; 9, Heft 1 (17.2.2017), 1-4, 12.2017
- Keyword
-
Erbkrankheit
Erbschaden
- Creator
-
Shah, Ruth R.
- Contributor
-
Bird, Adrian P.
SpringerLink (Online service)
- DOI
-
10.1186/s13073-017-0411-7
- URN
-
urn:nbn:de:1111-20170312994
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Shah, Ruth R.
- Bird, Adrian P.
- SpringerLink (Online service)
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Interplay between MeCP2 and BDNF in Rett Syndrome
MeCP2 and Chromatin Compartmentalization
Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets
Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome
Graded and pan-neural disease phenotypes of Rett Syndrome linked with dosage of functional MeCP2
Regulation of MeCP2 induced heterochromatin remodeling
Regulation of MeCP2 induced heterochromatin remodeling
Epigenetik der chronischen Herzinsuffizienz: Bedeutung von MeCP2
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