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PDFOnline mutation report
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)
- Correspondence to: Dr Carsten Bergmann Department of Human Genetics, Aachen University, Pauwelsstrasse 30, D-52074 Aachen, Germany; cbergmannukaachen.de
Citation
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)
Publication history
- Received February 22, 2005
- Accepted March 31, 2005
- Revised March 28, 2005
- First published September 30, 2005.
Online issue publication
September 30, 2005
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- [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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Copyright 2005 Journal of Medical Genetics