Whole-exome sequencing for finding de novo mutations in sporadic mental retardation

Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

Detalles Bibliográficos
Autor principal: Robinson, Peter N
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Highlight
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046476/
https://www.ncbi.nlm.nih.gov/pubmed/21172032
http://dx.doi.org/10.1186/gb-2010-11-12-144
Descripción
Sumario:Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

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