Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability

BACKGROUND: More than 30 genes can harbor rare exonic variants sufficient to cause nephrotic syndrome (NS), and the number of genes implicated in monogenic NS continues to grow. However, outside the first year of life, the majority of affected patients, particularly in ancestrally mixed populations,...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:Pediatr Nephrol
Main Authors: Crawford, Brendan D., Gillies, Christopher E., Robertson, Catherine C., Kretzler, Matthias, Otto, Edgar, Vega-Wagner, Virginia, Sampson, Matthew G.
Format: Artigo
Sprog:Inglês
Udgivet: 2016
Fag:
Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5483602/
https://ncbi.nlm.nih.gov/pubmed/27766458
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-016-3513-3
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker