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A novel SLC34A2 mutation in a patient with pulmonary alveolar microlithiasis
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive disease caused by mutations in SLC34A2 and characterized by intra-alveolar accumulation of microliths. We diagnosed a case of PAM in a 27-year-old Japanese female and identified a novel mutation in SLC34A2 (c.1390 G>C [G464R] i...
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| Udgivet i: | Hum Genome Var |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Nature Publishing Group
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5267164/ https://ncbi.nlm.nih.gov/pubmed/28144448 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2016.47 |
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