Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1999-6-30
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1059-7794
pubmed:author
pubmed:issnType
Print
pubmed:volume
Suppl 1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
S106-9
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:9452056-Adolescent, pubmed-meshheading:9452056-Adult, pubmed-meshheading:9452056-Amino Acid Sequence, pubmed-meshheading:9452056-Amino Acid Substitution, pubmed-meshheading:9452056-Child, pubmed-meshheading:9452056-Collagen, pubmed-meshheading:9452056-DNA, pubmed-meshheading:9452056-DNA Mutational Analysis, pubmed-meshheading:9452056-Female, pubmed-meshheading:9452056-Genetic Linkage, pubmed-meshheading:9452056-Humans, pubmed-meshheading:9452056-Male, pubmed-meshheading:9452056-Middle Aged, pubmed-meshheading:9452056-Molecular Sequence Data, pubmed-meshheading:9452056-Mutation, Missense, pubmed-meshheading:9452056-Nephritis, Hereditary, pubmed-meshheading:9452056-Point Mutation, pubmed-meshheading:9452056-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:9452056-Sequence Homology, Amino Acid, pubmed-meshheading:9452056-X Chromosome
pubmed:year
1998
pubmed:articleTitle
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome.
pubmed:affiliation
Cattedra di Genetica Medica, Università di Parma, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't