Wu, Chen-Han Wilfred
Mann, Nina
Nakayama, Makiko
Connaughton, Dervla M.
Dai, Rufeng
Kolvenbach, Caroline M.
Kause, Franziska
Ottlewski, Isabel
Wang, Chunyan
Klämbt, Verena
Seltzsam, Steve
Lai, Ethan W.
Selvin, Aravind
Senguttuva, Prabha
Bodamer, Olaf
Stein, Deborah R.
El Desoky, Sherif
Kari, Jameela A.
Tasic, Velibor
Bauer, Stuart B.
Shril, Shirlee
Hildebrandt, Friedhelm http://orcid.org/0000-0002-7130-0030
Funding for this research was provided by:
National Institutes of Health (DK088767, DK088767, DK088767)
Begg Family Foundation (-)
Deutsche Forschungsgemeinschaft (403877094)
This article is maintained by: Elsevier
Article Title: Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-020-0844-z
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics