ロード中...
Protein-losing enteropathy in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
BACKGROUND: Camptodactyly-arthropathy-coxa vara-pericarditis (CACP, OMIM: #208250) syndrome is a rare autosomal recessive disease that can be difficult to recognise not only because of its wide clinical variability but also because of its clinical resemblance to juvenile idiopathic arthritis (JIA)....
保存先:
| 出版年: | Pediatr Rheumatol Online J |
|---|---|
| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2016
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4880819/ https://ncbi.nlm.nih.gov/pubmed/27224999 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12969-016-0093-5 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|