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Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants
Amelogenesis imperfecta (AI) refers to a genetically and clinically heterogeneous group of inherited disorders affecting the structure, composition, and quantity of tooth enamel. Both non-syndromic and syndromic forms of AI have been described and several genes affecting various aspects of the ename...
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| Publicado no: | Hum Genet |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6536466/ https://ncbi.nlm.nih.gov/pubmed/30877375 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-019-01997-8 |
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