| Predicate |
Object |
| contentType |
Journal Article |
| endingPage |
1014 |
| issn |
0275-004X |
| issueIdentifier |
7 |
| pageRange |
1013-1014 |
| publicationName |
Retina (Philadelphia, Pa.) |
| startingPage |
1013 |
| bibliographicCitation |
Bass SJ, Noble KG. A Thr17Met mutation is associated with an unusual retinochoroidopathy in an autosomal dominant pedigree. Retina. 2008 Jul;28(7):1013–4. doi: 10.1097/iae.0b013e31816da918. PMID: 18698306. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_49690638b85892a69dc5d88ff1cc4c3f
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_595bc2e27df10dcda70967eb582aefdf |
| date |
200807 |
| identifier |
https://doi.org/10.1097/iae.0b013e31816da918
https://pubmed.ncbi.nlm.nih.gov/18698306 |
| isPartOf |
https://portal.issn.org/resource/ISSN/0275-004X
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/6933 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
A Thr17Met Mutation Is Associated With an Unusual Retinochoroidopathy in an Autosomal Dominant Pedigree |
| discusses |
http://id.nlm.nih.gov/mesh/M0019047 |
| hasPrimarySubjectTerm |
http://id.nlm.nih.gov/mesh/D015862Q000235
http://id.nlm.nih.gov/mesh/D012243Q000235
http://id.nlm.nih.gov/mesh/D020125
http://id.nlm.nih.gov/mesh/D012174Q000235 |
| hasSubjectTerm |
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D005799
http://id.nlm.nih.gov/mesh/D019943
http://id.nlm.nih.gov/mesh/D004252
http://id.nlm.nih.gov/mesh/D010375 |
| discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID597
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6288
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID876
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID84815
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_843a28dfdc5b2d5463ba2a7b83fdec7c
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1135
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9093
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6137 |