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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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| 出版年: | Animals (Basel) |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2021
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| 主題: | |
| オンライン・アクセス: | 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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