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Pulmonary alveolar microlithiasis with finger clubbing: A case report and literature review
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive and slowly progressive disease. Mutations of the solute carrier family 34, member 2 gene are considered to be the cause of the disease. The present study reported the case of a 35-year-old female patient who was diagnosed with PAM...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4812549/ https://ncbi.nlm.nih.gov/pubmed/27073453 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2016.3075 |
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