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rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
5
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pubmed:dateCreated |
1997-6-9
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|
pubmed:abstractText |
We describe a family with autosomal dominant polycystic kidney disease in which molecular typing with closely linked markers for the PKD1 and PKD2 genes indicated absence of linkage. Thus, a third still unknown locus appears likely to be involved in disease development. This is the fourth "PKD3-linked" family described to date and the first from Italy.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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pubmed:month |
Nov
|
|
pubmed:issn |
0272-6386
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
28
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
759-61
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:9158217-Adult,
pubmed-meshheading:9158217-Chromosome Mapping,
pubmed-meshheading:9158217-Chromosomes, Human, Pair 16,
pubmed-meshheading:9158217-Chromosomes, Human, Pair 4,
pubmed-meshheading:9158217-Female,
pubmed-meshheading:9158217-Genetic Linkage,
pubmed-meshheading:9158217-Haplotypes,
pubmed-meshheading:9158217-Humans,
pubmed-meshheading:9158217-Italy,
pubmed-meshheading:9158217-Male,
pubmed-meshheading:9158217-Middle Aged,
pubmed-meshheading:9158217-Pedigree,
pubmed-meshheading:9158217-Polycystic Kidney, Autosomal Dominant
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|
pubmed:year |
1996
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|
pubmed:articleTitle |
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene.
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pubmed:affiliation |
Institute of Genetics, University of Verona School of Medicine, University Hospital Polyclinic Borgo Roma, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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