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UnknownComprehensive genetic diagnosis of Japanese patients with severe proteinuria.
Not available
S-EPMC6959278 | biostudies-literature
UnknownClinical and Genetic Characteristics in Patients With Gitelman Syndrome.
Not available
S-EPMC6308995 | biostudies-literature
UnknownThe utility of urinary CD80 as a diagnostic marker in patients with renal diseases.
Not available
S-EPMC6251900 | biostudies-literature
UnknownNatural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome.
Not available
S-EPMC5733817 | biostudies-literature
UnknownLast Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing.
Not available
S-EPMC8720670 | biostudies-literature
UnknownComparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.
Not available
S-EPMC6732293 | biostudies-literature
UnknownPathogenic evaluation of synonymous COL4A5 variants in X-linked Alport syndrome using a minigene assay.
Not available
S-EPMC7434753 | biostudies-literature
UnknownClinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
Not available
S-EPMC8770369 | biostudies-literature
UnknownExamination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases.
Not available
S-EPMC8352941 | biostudies-literature
UnknownGlomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases.
Not available
S-EPMC7441388 | biostudies-literature
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