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Nature Genetics|February 11, 2014
Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndromeKálmán Tory, Dóra K Menyhárd, Stéphanie Woerner, et al.Plos One|January 19, 2012
Brain phenotype of transgenic mice overexpressing cystathionine β-synthaseVinciane Régnier, Jean-Marie Billard, Sapna Gupta, et al.Journal of the American Society of Nephrology : JASN|May 21, 2013
LMX1B mutations cause hereditary FSGS without extrarenal involvementOlivia Boyer, Stéphanie Woerner, Fan Yang, et al.Journal of the American Society of Nephrology : JASN|May 31, 2014
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGSEvelyne Huynh Cong, Albane A Bizet, Olivia Boyer, et al.Pageof 1