EXPLAIN Fragile-X: an explorative, longitudinal study on the characterization, treatment pathways, and patient-related outcomes of Fragile X Syndrome

BACKGROUND: Fragile X syndrome (FXS), caused by a mutation of the FMR1 gene on the X chromosome, is the most common inherited form of intellectual disability and autism spectrum disorders. Comprehensive data are lacking, however, on the characteristics and management patients with FXS in Germany. ME...

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Detalhes bibliográficos
Main Authors: Haessler, Frank, Gaese, Franziska, Colla, Michael, Huss, Michael, Kretschmar, Christoph, Brinkman, Marc, Schieb, Heike, Peters, Helmut, Elstner, Samuel, Pittrow, David
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Study Protocol
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3878315/
https://ncbi.nlm.nih.gov/pubmed/24354947
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-244X-13-339
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