UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly

PURPOSE: The human chromosome 19q13.11 deletion syndrome is associated with a variable phenotype that includes aplasia cutis congenita (ACC) and ectrodactyly as specific features. UBA2 (ubiquitin-like modifier-activating enzyme 2) lies adjacent to the minimal deletion overlap region. We aim to defin...

Descripción completa

Detalles Bibliográficos
Autores principales: Schnur, Rhonda E., Yousaf, Sairah, Liu, James, Chung, Wendy K., Rhodes, Lindsay, Marble, Michael, Zambrano, Regina M., Sobreira, Nara, Jayakar, Parul, Pierpont, Mary Ella, Schultz, Matthew J., Pichurin, Pavel N., Olson, Rory J., Graham, Gail E., Osmond, Matthew, Contreras-García, Gustavo A., Campo-Neira, Karina A, Peñaloza-Mantilla, Camilo A., Flage, Mark, Kuppa, Srikar, Navarro, Karina, Sacoto, Maria J. Guillen, Wentzensen, Ingrid M., Scarano, Maria I., Juusola, Jane, Prada, Carlos E., Hufnagel, Robert B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463496/
https://www.ncbi.nlm.nih.gov/pubmed/34040189
http://dx.doi.org/10.1038/s41436-021-01182-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463496/
https://www.ncbi.nlm.nih.gov/pubmed/34040189
http://dx.doi.org/10.1038/s41436-021-01182-1

Ejemplares similares