Associated Papers
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Riedhammer KM et al.
Kidney International, 2024
38154558 (PubMed )
Supplement: mmc2.xlsx › Family_1
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.
Suzuki K et al.
Nature Genetics, 2019
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