| Predicate |
Object |
| contentType |
Journal Article |
| endingPage |
400 |
| issn |
1059-7794
1098-1004 |
| issueIdentifier |
4 |
| pageRange |
399-400 |
| publicationName |
Human Mutation |
| startingPage |
399 |
| bibliographicCitation |
Aulehla-Scholz C, Heilbronner H. Mutational spectrum in German patients with phenylalanine hydroxylase deficiency. Hum Mutat. 2003 Apr;21(4):399–400. doi: 10.1002/humu.9116. PMID: 12655553. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0f1492a334a2c416de4927f0e9a0e414
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5bd80ac3ae2af057870aa51026698b2e |
| date |
2003-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1002/humu.9116
https://pubmed.ncbi.nlm.nih.gov/12655553 |
| isPartOf |
https://portal.issn.org/resource/ISSN/1059-7794
https://portal.issn.org/resource/ISSN/1098-1004
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/2408 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Mutational spectrum in German patients with phenylalanine hydroxylase deficiency |
| discusses |
http://id.nlm.nih.gov/mesh/M0016546 |
| hasPrimarySubjectTerm |
http://id.nlm.nih.gov/mesh/D010651Q000172
http://id.nlm.nih.gov/mesh/D010651Q000235 |
| hasSubjectTerm |
http://id.nlm.nih.gov/mesh/D005828
http://id.nlm.nih.gov/mesh/D005820
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D008297
http://id.nlm.nih.gov/mesh/D014421Q000208
http://id.nlm.nih.gov/mesh/D004252
http://id.nlm.nih.gov/mesh/D005260
http://id.nlm.nih.gov/mesh/D005858Q000453
http://id.nlm.nih.gov/mesh/D005787Q000235
http://id.nlm.nih.gov/mesh/D006580 |
| discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8868
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9264
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_ab7136ba08704e4eb4a19169e1a26695
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/EC_1.14.16.1 |