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9199930
Source:
http://linkedlifedata.com/resource/pubmed/id/9199930
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017337
,
umls-concept:C0017428
,
umls-concept:C0026882
,
umls-concept:C0029246
,
umls-concept:C0086418
,
umls-concept:C0733682
,
umls-concept:C1418526
pubmed:issue
6
pubmed:dateCreated
1997-9-15
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AJ001637
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08111
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08112
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08113
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08114
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08115
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08116
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08117
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08118
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08119
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08120
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08121
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08122
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08123
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08124
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08125
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08126
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08127
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08128
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08129
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08130
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08131
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y08132
,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Y10196
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9518021
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Codon, Nonsense
,
http://linkedlifedata.com/resource/pubmed/chemical/Neprilysin
,
http://linkedlifedata.com/resource/pubmed/chemical/PHEX Phosphate Regulating Neutral...
,
http://linkedlifedata.com/resource/pubmed/chemical/PHEX protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1088-9051
pubmed:author
pubmed-author:BöddrichAA
,
pubmed-author:BorzymKK
,
pubmed-author:BrandaoAA
,
pubmed-author:CagnoliMM
,
pubmed-author:EconsM JMJ
,
pubmed-author:FranciaPP
,
pubmed-author:HennigSS
,
pubmed-author:KlagesSS
,
pubmed-author:LehrachHH
,
pubmed-author:LorenzBB
,
pubmed-author:MeitingerTT
,
pubmed-author:MohnikeK LKL
,
pubmed-author:OudetCC
,
pubmed-author:PohlTT
,
pubmed-author:ReinhardtRR
,
pubmed-author:RoweP SPS
,
pubmed-author:SteffensCC
,
pubmed-author:StromT MTM
pubmed:issnType
Print
pubmed:volume
7
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
573-85
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9199930-Cloning, Molecular
,
pubmed-meshheading:9199930-Codon, Nonsense
,
pubmed-meshheading:9199930-Exons
,
pubmed-meshheading:9199930-Female
,
pubmed-meshheading:9199930-Frameshift Mutation
,
pubmed-meshheading:9199930-Genetic Variation
,
pubmed-meshheading:9199930-Humans
,
pubmed-meshheading:9199930-Hypophosphatemia, Familial
,
pubmed-meshheading:9199930-Introns
,
pubmed-meshheading:9199930-Male
,
pubmed-meshheading:9199930-Molecular Sequence Data
,
pubmed-meshheading:9199930-Mutation
,
pubmed-meshheading:9199930-Neprilysin
,
pubmed-meshheading:9199930-PHEX Phosphate Regulating Neutral Endopeptidase
,
pubmed-meshheading:9199930-Pedigree
,
pubmed-meshheading:9199930-Proteins
,
pubmed-meshheading:9199930-Sequence Analysis, DNA
,
pubmed-meshheading:9199930-Sequence Deletion
,
pubmed-meshheading:9199930-Sequence Homology, Nucleic Acid
pubmed:year
1997
pubmed:articleTitle
Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.
pubmed:affiliation
Max-Planck Institut für Molekulare Genetik, Berlin, Germany. francis@mpimg-berlin-dahlem.mpg.de
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't