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Pulmonary alveolar microlithiasis: A report of two unique cases
Pulmonary alveolar microlithiasis (PAM) is an inherited autosomal recessive disease. PAM is classically characterized by calcium phosphate deposition within alveolar airspaces due to SLC34A2 (solute carrier family 34 member 2) gene mutation located on chromosome 4p15.2. Such cellular genetic mutatio...
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| 出版年: | Respir Med Case Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Elsevier
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6928350/ https://ncbi.nlm.nih.gov/pubmed/31890557 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2019.100980 |
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