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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Detalles Bibliográficos
Autores principales: Oh, Taehoon, Jung Seo, Hyun, Taek Lee, Kyu, Jo Kim, Han, Jun Kim, Hwi, Lee, Ji-Hye, Il Cheong, Hae, Young Lee, Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570591/
https://www.ncbi.nlm.nih.gov/pubmed/26484020
http://dx.doi.org/10.1016/j.krcp.2014.09.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570591/
https://www.ncbi.nlm.nih.gov/pubmed/26484020
http://dx.doi.org/10.1016/j.krcp.2014.09.003

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