Pkd mutations and evaluation of same (U.S. Patent Number 20100047785 A1)

Acronym: Not Available NIDDK Contact: Principal Investigator(s): Gregory Germino


The present invention relates to methods of detecting novel mutations in a PKD1 and/or PKD2 gene that have been determined to be associated with autosomal dominant polycystic kidney disease (ADPKD) in order to detect or predict the occurrence of ADPKD in an individual.

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