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C1q Nephropathy in a Patient of Neurofibromatosis Type 1: A Rare Case Report

C1q nephropathy is a rare glomerular disease defined by the presence of characteristic mesangial dominant or codominant C1q deposition on immunofluorescence microscopy. Neurofibromatosis type 1 (NF-1) is an autosomal dominant syndrome caused by a mutation of a gene located on chromosomal segment 17q...

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Detalles Bibliográficos
Autores principales:	Varyani, U. T., Shah, N. M., Shah, P. R., Kute, V. B., Balwani, M. R., Trivedi, H. L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2019
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440327/ https://www.ncbi.nlm.nih.gov/pubmed/30983754 http://dx.doi.org/10.4103/ijn.IJN_353_17

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