Pages that link to "Q42217620"
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The following pages link to Splicing defects caused by exonic mutations in PKD1 as a new mechanism of pathogenesis in autosomal dominant polycystic kidney disease (Q42217620):
Displaying 5 items.
- Molecular and functional characterization of the BMPR2 gene in Pulmonary Arterial Hypertension (Q33689573) (← links)
- Functional analysis by minigene assay of putative splicing variants found in Bardet-Biedl syndrome patients. (Q38787335) (← links)
- Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease (Q47558855) (← links)
- Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants (Q56967912) (← links)
- Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease (Q90451238) (← links)