Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1994-10-10
pubmed:databankReference
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1059-7794
pubmed:author
pubmed:issnType
Print
pubmed:volume
3
pubmed:geneSymbol
COL4A5
pubmed:owner
NLM
pubmed:authorsComplete
N
pubmed:pagination
386-90
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8081393-Adenine Nucleotides, pubmed-meshheading:8081393-Adult, pubmed-meshheading:8081393-Amino Acid Sequence, pubmed-meshheading:8081393-Base Sequence, pubmed-meshheading:8081393-Child, pubmed-meshheading:8081393-Collagen, pubmed-meshheading:8081393-DNA, Single-Stranded, pubmed-meshheading:8081393-DNA Mutational Analysis, pubmed-meshheading:8081393-DNA Primers, pubmed-meshheading:8081393-Female, pubmed-meshheading:8081393-Frameshift Mutation, pubmed-meshheading:8081393-Humans, pubmed-meshheading:8081393-Male, pubmed-meshheading:8081393-Molecular Sequence Data, pubmed-meshheading:8081393-Nephritis, Hereditary, pubmed-meshheading:8081393-Nucleic Acid Conformation, pubmed-meshheading:8081393-Nucleic Acid Heteroduplexes, pubmed-meshheading:8081393-Pedigree, pubmed-meshheading:8081393-Polymorphism, Genetic
pubmed:year
1994
pubmed:articleTitle
A novel frameshift deletion in type IV collagen alpha 5 gene in a juvenile-type Alport syndrome patient: an adenine deletion (2940/2943 del A) in exon 34 of COL4A5.
pubmed:affiliation
Institute of Biological Sciences and Genetics, University of Verona School of Medicine, University Hospital Polyclinic, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't