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The WNT10A gene in Ectodermal Dysplasias and Selective Tooth Agenesis
Mutations in the WNT10A gene were first detected in the rare syndrome odonto-onycho-dermal dysplasia (OODD, OMIM257980) but have now also been found to cause about 35-50% of selective tooth agenesis (STHAG4, OMIM150400), a common disorder that mostly affects the permanent dentition. In our random sa...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4167166/ https://ncbi.nlm.nih.gov/pubmed/24700731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.36520 |
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