A carregar...
Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta
The conventional approach to identifying the defective gene in a family with an inherited disease is to find the disease locus through family studies. However, the rapid development and decreasing cost of next generation sequencing facilitates a more direct approach. Here, we report the identificati...
Na minha lista:
| Main Authors: | , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2014
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3865405/ https://ncbi.nlm.nih.gov/pubmed/23632796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.76 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|