Prevalence of clinical, pathological and molecular features of glomerular basement membrane nephropathy caused by COL4A3 or COL4A4 mutations: a systematic review

BACKGROUND: Patients heterozygous for COL4A3 or COL4A4 mutations show a wide spectrum of disease, extending from familial isolated microscopic haematuria, as a result of thin basement membranes (TBMs), to autosomal dominant Alport syndrome (ADAS) and end-stage renal disease (ESRD). Many patients are...

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Detalles Bibliográficos
Autores principales: Matthaiou, Andreas, Poulli, Tsielestina, Deltas, Constantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769542/
https://www.ncbi.nlm.nih.gov/pubmed/33391746
http://dx.doi.org/10.1093/ckj/sfz176

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769542/
https://www.ncbi.nlm.nih.gov/pubmed/33391746
http://dx.doi.org/10.1093/ckj/sfz176

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