Associated Papers
Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux.
Bartik ZI et al.
Plos One, 2022
36417404 (PubMed )
Supplement: pone.0277524.s006.xlsx › Supplemental_table_S4
Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Töpf A et al.
Plos One, 2014
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