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Object |
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Journal Article|Research Support, Non-U.S. Gov't |
| endingPage |
1221 |
| issn |
1530-8561
0009-9147 |
| issueIdentifier |
7 |
| pageRange |
1216-1221 |
| publicationName |
Clinical Chemistry |
| startingPage |
1216 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a00fabcde302d63a76ef3eae515fd4ec |
| bibliographicCitation |
Williams E, Rumsby G. Selected exonic sequencing of the AGXT gene provides a genetic diagnosis in 50% of patients with primary hyperoxaluria type 1. Clin Chem. 2007 Jul;53(7):1216–21. doi: 10.1373/clinchem.2006.084434. PMID: 17495019. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ce109212410b59d49021814efcf5bf19
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d960b1959e45e86a9f65e81bb3a15b40 |
| date |
2007-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1373/clinchem.2006.084434
https://pubmed.ncbi.nlm.nih.gov/17495019 |
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https://portal.issn.org/resource/ISSN/0009-9147
https://portal.issn.org/resource/ISSN/1530-8561
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/2992 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Selected Exonic Sequencing of the AGXT Gene Provides a Genetic Diagnosis in 50% of Patients with Primary Hyperoxaluria Type 1 |
| discusses |
http://id.nlm.nih.gov/mesh/M0072267
http://id.nlm.nih.gov/mesh/M0359363
http://id.nlm.nih.gov/mesh/M0000972 |
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http://id.nlm.nih.gov/mesh/D000637Q000235 |
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http://id.nlm.nih.gov/mesh/D017422
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http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID1127 |