Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4

BACKGROUND: Coffin–Siris syndrome (CSS) is characterized by intellectual disability, dysmorphic facial features, growth deficiency, microcephaly, and abnormalities of the fifth fingers/toes. CSS is caused by mutations in several genes of the BRG1‐associated factor pathway including SMARCA4. METHODS:...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Mol Genet Genomic Med
Autores principales: Cappuccio, Gerarda, Brunetti‐Pierri, Raffaella, Torella, Annalaura, Pinelli, Michele, Castello, Raffaele, Casari, Giorgio, Nigro, Vincenzo, Banfi, Sandro, Simonelli, Francesca, Brunetti‐Pierri, Nicola
Formato: Artigo
Lenguaje:Inglês
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6565552/
https://ncbi.nlm.nih.gov/pubmed/30973214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.682
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares