A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype

BACKGROUND: Intellectual disability (ID) is a feature of many rare diseases caused by thousands of genes. This genetic heterogeneity implies that pathogenic variants in a specific gene are found only in a small number of patients, and difficulties arise in the definition of prevailing genotype and c...

Descripción completa

Detalles Bibliográficos
Autores principales: Hancarova, Miroslava, Babikyan, Davit, Bendova, Sarka, Midyan, Susanna, Prchalova, Darina, Shahsuvaryan, Gohar, Stranecky, Viktor, Sarkisian, Tamara, Sedlacek, Zdenek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732288/
https://www.ncbi.nlm.nih.gov/pubmed/31334606
http://dx.doi.org/10.1002/mgg3.865

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732288/
https://www.ncbi.nlm.nih.gov/pubmed/31334606
http://dx.doi.org/10.1002/mgg3.865

Ejemplares similares