Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series

BACKGROUND: Genetic risk variants in the hemizygous allele may influence neuropsychiatric manifestations and clinical course in 3q29 deletion carriers. METHODS: In‐depth phenotypic assessment in two deletion carriers included medical records, medical, genetic, psychiatric and neuropsychological eval...

Descripción completa

Detalles Bibliográficos
Autores principales: Malt, Eva Albertsen, Juhasz, Katalin, Frengen, Anna, Wangensteen, Teresia, Emilsen, Nina Merete, Hansen, Borre, Agafonov, Oleg, Nilsen, Hilde Loge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732294/
https://www.ncbi.nlm.nih.gov/pubmed/31347308
http://dx.doi.org/10.1002/mgg3.889

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732294/
https://www.ncbi.nlm.nih.gov/pubmed/31347308
http://dx.doi.org/10.1002/mgg3.889

Ejemplares similares