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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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| Gepubliceerd in: | Respir Med Case Rep |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2019
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| Onderwerpen: | |
| Online toegang: | 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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