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pubmed-article:16199545pubmed:abstractTextAutosomal recessive polycystic kidney disease (ARPKD) is caused by mutations in the PKHD1 (polycystic kidney and hepatic disease 1) gene on chromosome 6p12, a large gene spanning 470 kb of genomic DNA. So far, only micromutations in the 66 exons encoding the longest open reading frame (ORF) have been described, and account for about 80% of mutations.lld:pubmed
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pubmed-article:16199545pubmed:articleTitleMulti-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD).lld:pubmed
pubmed-article:16199545pubmed:affiliationDepartment of Human Genetics, Aachen University, Germany. cbergmann@ukaachen.delld:pubmed
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