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A De Novo Mutation in COL1A1 in a Holstein Calf with Osteogenesis Imperfecta Type II
SIMPLE SUMMARY: Skeletal connective tissue disorders represent a heterogeneous group of inherited disorders mostly monogenically inherited. Heritable connective tissue disorders such as osteogenesis imperfecta (OI) belong to this group. Herein, an affected calf showing congenital bone lesions such a...
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| Publicado no: | Animals (Basel) |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7924654/ https://ncbi.nlm.nih.gov/pubmed/33672767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ani11020561 |
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