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Target gene analyses of 39 amelogenesis imperfecta kindreds
Previously, mutational analyses identified six disease-causing mutations in 24 amelogenesis imperfecta (AI) kindreds. We have since expanded the number of AI kindreds to 39, and performed mutation analyses covering the coding exons and adjoining intron sequences for the six proven AI candidate genes...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3292789/ https://ncbi.nlm.nih.gov/pubmed/22243262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1600-0722.2011.00857.x |
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