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Myosin Heavy Chain 9 (MYH9)-Related Congenital Macrothrombocytopenia

Myosin heavy chain 9 (MYH9)-related hereditary macrothrombocytopenia is caused by mutation of the MYH9 gene encoding the heavy chain A of non-muscle myosin of class II. We present a case that emphasizes the importance of awareness of rare disorders which could potentially avoid over-investigation, e...

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Detalles Bibliográficos
Autores principales:	Thurlapati, Aswani, Guntupalli, Srinandan, Mansour, Richard
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2021
Materias:	Internal Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419368/ https://www.ncbi.nlm.nih.gov/pubmed/34527454 http://dx.doi.org/10.7759/cureus.16964

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