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Critical appraisal of genotype assessment in molybdenum cofactor deficiency.

Katrin HinderhoferKonstantin MechlerGeorg F HoffmannAnette LampertWilliam K MountfordMarkus Ries
Published in: Journal of inherited metabolic disease (2017)
The severity of the genotype assessed by in silico prediction and further classification explained survival in molybdenum cofactor deficiency and may therefore be considered a confounder for the outcome of therapeutic clinical trials requiring adjustment in the clinical trial design or analysis. These results should further be investigated by future in vitro or in vivo functional studies. Caution should be taken with this approach for the classification of variants in molecular genetic diagnostics or genetic counseling.
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