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MYH9 Genetic Variants Associated With Glomerular Disease: What Is the Role for Genetic Testing?
Genetic variation in MYH9, encoding nonmuscle myosin IIA heavy chain, has been associated recently with increased risk for kidney disease. Previously, MYH9 missense mutations have been shown to cause the autosomal-dominant MYH9 (ADM9) spectrum, characterized by large platelets, leukocyte Döhle bodie...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3097395/ https://ncbi.nlm.nih.gov/pubmed/20807613 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.semnephrol.2010.06.007 |
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