The phenotypical implications of immune dysregulation in fragile X syndrome.

Yu, K-H; Palmer, N; Fox, K; Prock, L; Mandl, K D; Kohane, I S; Prilutsky, D

Yu, K-H; Palmer, N; Fox, K; Prock, L; Mandl, K D; Kohane, I S; Prilutsky, D.

Afiliación

Yu KH; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts, USA.
Palmer N; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts, USA.
Fox K; Aetna Inc., Hartford, Connecticut, USA.
Prock L; Division of Developmental Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Mandl KD; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts, USA.
Kohane IS; Computational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts, USA.
Prilutsky D; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts, USA.

Eur J Neurol ; 27(3): 590-593, 2020 03.

Article en En | MEDLINE | ID: mdl-31953887

Asunto(s)

Síndrome del Cromosoma X Frágil/inmunología; Estudios de Cohortes; Comorbilidad; Bases de Datos Factuales; Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil/genética; Humanos; Fenotipo

Palabras clave

genetic and inherited disorders; intellectual disability; trinucleotide repeat diseases

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google