Refinement of the Gene Locus for Autosomal Dominant Medullary Cystic Kidney Disease Type 1 (MCKD1) and Construction of a Physical and Partial Transcriptional Map of the Region
- 15 March 2001
- Vol. 72 (3) , 278-284
- https://doi.org/10.1006/geno.2000.6486
Abstract
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This publication has 29 references indexed in Scilit:
- Molecular Cloning of the Critical Region for Glomerulopathy with Fibronectin Deposits (GFND) and Evaluation of Candidate GenesGenomics, 2000
- Construction of a Gene Map of the Nephronophthisis Type 1 (NPHP1) Region on Human Chromosome 2q12–q13Genomics, 1998
- A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1Nature Genetics, 1997
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Hepatocyte growth factor in nephronophthisis-medullary cystic disease complexPediatric Nephrology, 1996
- The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritanceNature Genetics, 1995
- The Interferon-Inducible, Double-Stranded RNA-Specific Adenosine Deaminase Gene (DSRAD) Maps to Human Chromosome 1q21.1–21.2Genomics, 1995
- A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyNature Genetics, 1995
- Physical Mapping of a Functional Cluster of Epidermal Differentiation Genes on Chromosome 1q21Genomics, 1993
- A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association.Journal of Clinical Investigation, 1984