Associated Papers
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.
Ahram DF et al.
Journal of the American Society of Nephrology : Jasn, 2023
Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis.
Vidic C et al.
Molecular and Cellular Pediatrics, 2021
34608560 (PubMed )
Supplement: 40348_2021_122_MOESM4_ESM.xlsx › Tabelle1
Mutations in DSTYK and dominant urinary tract malformations.
Sanna-Cherchi S et al.
The New England Journal of Medicine, 2013
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