On new hypotheses about autosomal dominant polycystic kidney disease type 1
Open Access
- 31 December 2001
- journal article
- Published by Elsevier in Medical Hypotheses
- Vol. 57 (6) , 754-758
- https://doi.org/10.1054/mehy.2001.1482
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Genome Duplications and Other Features in 12 Mb of DNA Sequence from Human Chromosome 16p and 16qGenomics, 1999
- Are Only Repeated Triplets Guilty?Journal of Theoretical Biology, 1998
- Gene conversion is a likely cause of mutation in PKD1Human Molecular Genetics, 1998
- Novel and recurrent mutations in the PKD1 (Polycystic Kidney disease) geneHuman Genetics, 1998
- PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane ProteinScience, 1996
- Autosomal dominant polycystic kidney disease: molecular analysisHuman Molecular Genetics, 1995
- Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeatHuman Molecular Genetics, 1995
- Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletionHuman Molecular Genetics, 1995
- Polycystic kidney disease: The complete structure of the PKD1 gene and its proteinCell, 1995
- Is there evidence for anticipation in autosomal-dominant polycystic kidney disease?Kidney International, 1994