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CAFFEY DISEASE: NEW PERSPECTIVES ON OLD QUESTIONS
The autosomal dominant form of Caffey disease is a largely self-limiting infantile bone disorder characterized by acute inflammation of soft tissues and localized thickening of the underlying bone cortex. It is caused by a recurrent arginine-to-cysteine substitution (R836C) in the α1(I) chain of typ...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3987944/ https://ncbi.nlm.nih.gov/pubmed/24389367 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2013.12.030 |
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