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Object |
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Case Reports|Journal Article |
| endingPage |
395 |
| issn |
1744-5094
1381-6810 |
| issueIdentifier |
3 |
| pageRange |
391-395 |
| publicationName |
Ophthalmic Genetics |
| startingPage |
391 |
| bibliographicCitation |
Gumus E. Case report of four siblings in southeast Turkey with a novel RAB3GAP2 splice site mutation: Warburg micro syndrome or Martsolf syndrome? Ophthalmic Genet. 2018 Jun;39(3):391–5. doi: 10.1080/13816810.2018.1432065. PMID: 29419336. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-9932-0730 |
| date |
2018-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://pubmed.ncbi.nlm.nih.gov/29419336
https://doi.org/10.1080/13816810.2018.1432065 |
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| language |
English |
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https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Case report of four siblings in southeast Turkey with a novel RAB3GAP2 splice site mutation: Warburg micro syndrome or Martsolf syndrome? |
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