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Studies of the DMP1 57-kDa Functional Domain both in vivo and in vitro
Dmp1-null mice and patients with mutations in dentin matrix protein 1 (DMP1) resulting in autosomal recessive hypophosphatemic rickets display similar skeletal defects. As mutations were observed in the last 18 amino acids of DMP1 in 1 subset of patients and as fragments of intact DMP1, a 37-kDa N-t...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2667139/ https://ncbi.nlm.nih.gov/pubmed/18728349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000151727 |
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