Ubiquitous neurocognitive dysfunction in familial adenomatous polyposis: proof-of-concept of the role of APC protein in neurocognitive function

BACKGROUND: Familial adenomatous polyposis (FAP) is an autosomal dominant disorder caused by germline mutations in the APC gene. Patients with FAP have multiple extraintestinal manifestations that follow a genotype-phenotype pattern; however, few data exist characterizing their cognitive abilities....

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Detalles Bibliográficos
Autores principales: Cruz-Correa, Marcia Roxana, Sala, Ana Cecilia, Cintrón, Beatriz, Hernández, Jessica, Olivera, Myrta, Cora, Adrian, Moore, Constance M., Luciano, Carlos A., Soto-Salgado, Marievelisse, Giardiello, Francis M., Hooper, Stephen R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041079/
https://www.ncbi.nlm.nih.gov/pubmed/32123549
http://dx.doi.org/10.1186/s13053-020-0135-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041079/
https://www.ncbi.nlm.nih.gov/pubmed/32123549
http://dx.doi.org/10.1186/s13053-020-0135-3

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