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Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability
Brendan Crawford, Christopher E. Gillies, Catherine C. Robertson, Matthias Kretzler, Edgar Otto, Virginia Vega-Warner, Hyun Min Kang, Matthew G. Sampson
doi: https://doi.org/10.1101/071639
Brendan Crawford
Department of Pediatrics, University of Michigan Medical School
M.D., M.S.Christopher E. Gillies
Ph.D.
Catherine C. Robertson
M.S.
Matthias Kretzler
M.D.
Edgar Otto
Ph.D.
Virginia Vega-Warner
Ph.D.
Hyun Min Kang
Ph.D.
Matthew G. Sampson
M.D., M.S.C.E.
Article usage
Posted August 25, 2016.
Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability
Brendan Crawford, Christopher E. Gillies, Catherine C. Robertson, Matthias Kretzler, Edgar Otto, Virginia Vega-Warner, Hyun Min Kang, Matthew G. Sampson
bioRxiv 071639; doi: https://doi.org/10.1101/071639
Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability
Brendan Crawford, Christopher E. Gillies, Catherine C. Robertson, Matthias Kretzler, Edgar Otto, Virginia Vega-Warner, Hyun Min Kang, Matthew G. Sampson
bioRxiv 071639; doi: https://doi.org/10.1101/071639
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