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Opportunities and challenges of genotyping of patients with nephrotic syndrome in the genomic era

Both targeted and genome-wide linkage and association studies have identified a number of genes and genetic variants associated with nephrotic syndrome (NS). Genotype-phenotype studies of subjects with these variants have identified correlations of clear clinical significance. This, combined with im...

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Detalhes bibliográficos
Publicado no:Semin Nephrol
Main Authors: Sampson, Matthew G., Pollak, Martin R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4745990/
https://ncbi.nlm.nih.gov/pubmed/26215859
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.semnephrol.2015.04.002
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