Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2009-3-30
pubmed:abstractText
To estimate an accurate incidence rate for CYP1B1 mutations in German patients with primary congenital glaucoma (PCG).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1879-1891
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
147
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
744-53
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:19195637-Adult, pubmed-meshheading:19195637-Amino Acid Sequence, pubmed-meshheading:19195637-Aryl Hydrocarbon Hydroxylases, pubmed-meshheading:19195637-Chromatography, High Pressure Liquid, pubmed-meshheading:19195637-Cytochrome P-450 Enzyme System, pubmed-meshheading:19195637-DNA Mutational Analysis, pubmed-meshheading:19195637-European Continental Ancestry Group, pubmed-meshheading:19195637-Female, pubmed-meshheading:19195637-Germany, pubmed-meshheading:19195637-Glaucoma, pubmed-meshheading:19195637-Humans, pubmed-meshheading:19195637-Incidence, pubmed-meshheading:19195637-Male, pubmed-meshheading:19195637-Molecular Biology, pubmed-meshheading:19195637-Molecular Sequence Data, pubmed-meshheading:19195637-Mutation, pubmed-meshheading:19195637-Phenotype, pubmed-meshheading:19195637-Polymerase Chain Reaction, pubmed-meshheading:19195637-Polymorphism, Restriction Fragment Length, pubmed-meshheading:19195637-Polymorphism, Single Nucleotide, pubmed-meshheading:19195637-Sequence Analysis, DNA
pubmed:year
2009
pubmed:articleTitle
A clinical and molecular genetic study of German patients with primary congenital glaucoma.
pubmed:affiliation
Centre for Ophthalmology, Institute for Ophthalmic Research, Molecular Genetics Laboratory, Tuebingen, Germany. nicole.weisschuh@uni-tuebingen.de
pubmed:publicationType
Journal Article