Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome

Cornelia de Lange Syndrome (CdLS) is a choesinopathy: a severe genetic disorder caused by mutations in the cohesin complex genes. The phenotype is characterized by typical facial dysmorphism, growth impairment and multiorgan abnormalities including brain alterations. Wnt pathway is known to play a f...

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Detalles Bibliográficos
Autores principales: Avagliano, Laura, Grazioli, Paolo, Mariani, Milena, Bulfamante, Gaetano P., Selicorni, Angelo, Massa, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696803/
https://www.ncbi.nlm.nih.gov/pubmed/29162129
http://dx.doi.org/10.1186/s13023-017-0723-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696803/
https://www.ncbi.nlm.nih.gov/pubmed/29162129
http://dx.doi.org/10.1186/s13023-017-0723-0

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