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Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)
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  1. Correspondence to:
 Dr Carsten Bergmann
 Department of Human Genetics, Aachen University, Pauwelsstrasse 30, D-52074 Aachen, Germany; cbergmannukaachen.de
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Citation

Bergmann C, Küpper F, Schmitt CP, et al
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)
Online issue publication 
September 30, 2005
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    Files in this Data Supplement:

    • [view PDF] - Table S1. Primers and DHPLC conditions for alternate PKHD1 exons.
    • [view PDF] - Table S2. Primers Quantitative Real-Time PCR.

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