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MYH9 nephropathy
MYH9-related disorder is an autosomal dominant disease caused by a mutation in the MYH9 gene, which encodes nonmuscle myosin heavy chain IIA (NMMHC-IIA). This disease is characterized by giant platelets, thrombocytopenia, granulocyte inclusion bodies, proteinuria, and high-pitch sensorineural deafne...
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| Izdano u: | Kidney Res Clin Pract |
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| Glavni autori: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Elsevier
2015
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4570591/ https://ncbi.nlm.nih.gov/pubmed/26484020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.krcp.2014.09.003 |
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