Pseudodominant Alport syndrome caused by pathogenic homozygous and compound heterozygous COL4A3 splicing variants

The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials. Further phenotypic or sequencing data are available from the corresponding author (JAS), upon reasonable request. The identified genetic variant in COL4A3 have been submitted to LOVD (#0000478196 and #0000478197).

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