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than 700 variants have been described and a further 400 are estimated to be known to individual laboratories but are unpublished.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 |
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