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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Detalhes bibliográficos
Publicado no:Kidney Res Clin Pract
Main Authors: Oh, Taehoon, Jung Seo, Hyun, Taek Lee, Kyu, Jo Kim, Han, Jun Kim, Hwi, Lee, Ji-Hye, Il Cheong, Hae, Young Lee, Eun
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2015
Assuntos:
Case Report
Acesso em linha: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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