MYH9-related disorders display heterogeneous kidney involvement and outcome

BACKGROUND: MYH9-related diseases (MYH9-RD) are autosomal dominant disorders caused by mutations of the MYH9 gene encoding the non-muscle myosin heavy chain IIA. They are characterized by congenital thrombocytopenia, giant platelets and leucocyte inclusions. Hearing impairment, pre-senile cataract a...

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Detalles Bibliográficos
Autores principales: Tabibzadeh, Nahid, Fleury, Dominique, Labatut, Delphine, Bridoux, Frank, Lionet, Arnaud, Jourde-Chiche, Noémie, Vrtovsnik, François, Schlegel, Nicole, Vanhille, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Familial Nephropathy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6671426/
https://www.ncbi.nlm.nih.gov/pubmed/31384440
http://dx.doi.org/10.1093/ckj/sfy117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6671426/
https://www.ncbi.nlm.nih.gov/pubmed/31384440
http://dx.doi.org/10.1093/ckj/sfy117

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