DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome

X-linked Alport syndrome is a form of progressive renal failure caused by pathogenic variants in the COL4A5 gene. More than 700 variants have been described and a further 400 are estimated to be known to individual laboratories but are unpublished. The major genetic testing laboratories for X-linked...

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Veröffentlicht in:Pediatric nephrology (Berlin, West) West), 2014-06, Vol.29 (6), p.971-977
Hauptverfasser: Savige, Judy, Ars, Elisabet, Cotton, Richard G. H., Crockett, David, Dagher, Hayat, Deltas, Constantinos, Ding, Jie, Flinter, Frances, Pont-Kingdon, Genevieve, Smaoui, Nizar, Torra, Roser, Storey, Helen
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