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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Haessler, Frank, Gaese, Franziska, Colla, Michael, Huss, Michael, Kretschmar, Christoph, Brinkman, Marc, Schieb, Heike, Peters, Helmut, Elstner, Samuel, Pittrow, David
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2013
Aiheet:
Study Protocol
Linkit: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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