Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

BACKGROUND: Whole-exome sequencing has identified the causes of several Mendelian diseases by analyzing multiple unrelated cases, but it is more challenging to resolve the cause of extremely rare and suspected Mendelian diseases from individual families. We identified a family quartet with two child...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Kai, Kim, Cecilia, Bradfield, Jonathan, Guo, Yunfei, Toskala, Elina, Otieno, Frederick G, Hou, Cuiping, Thomas, Kelly, Cardinale, Christopher, Lyon, Gholson J, Golhar, Ryan, Hakonarson, Hakon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971341/
https://www.ncbi.nlm.nih.gov/pubmed/23889995
http://dx.doi.org/10.1186/gm471

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971341/
https://www.ncbi.nlm.nih.gov/pubmed/23889995
http://dx.doi.org/10.1186/gm471

Ejemplares similares