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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.
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| Formato: | Texto |
| Lenguaje: | English |
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BioMed Central
2010
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| 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 |