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Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfecta
BACKGROUND: Amelogenesis imperfecta (AI) is an inherited disorder characterized by abnormal formation of tooth enamel. Although several genes responsible for AI have been reported, not all causative genes for human AI have been identified to date. AMI rat has been reported as an autosomal recessive...
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| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2012
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3464675/ https://ncbi.nlm.nih.gov/pubmed/22676574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-7-34 |
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