The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1
| Main Authors: | , , , , , , |
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| Format: | Conference item |
| Language: | English |
| Published: |
Association for Research in Vision and Ophthalmology
2018
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| _version_ | 1826302470950748160 |
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| author | Yusuf, IH Gliem, M Birtel, J Muller, PL Mangold, E Bolz, H Issa, PC |
| author_facet | Yusuf, IH Gliem, M Birtel, J Muller, PL Mangold, E Bolz, H Issa, PC |
| author_sort | Yusuf, IH |
| collection | OXFORD |
| description | |
| first_indexed | 2024-03-07T05:48:02Z |
| format | Conference item |
| id | oxford-uuid:e7e1cf3f-319d-405a-bb7e-4ad69c0a7ae3 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T05:48:02Z |
| publishDate | 2018 |
| publisher | Association for Research in Vision and Ophthalmology |
| record_format | dspace |
| spelling | oxford-uuid:e7e1cf3f-319d-405a-bb7e-4ad69c0a7ae32022-03-27T10:42:27ZThe retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1Conference itemhttp://purl.org/coar/resource_type/c_5794uuid:e7e1cf3f-319d-405a-bb7e-4ad69c0a7ae3EnglishSymplectic ElementsAssociation for Research in Vision and Ophthalmology2018Yusuf, IHGliem, MBirtel, JMuller, PLMangold, EBolz, HIssa, PC |
| spellingShingle | Yusuf, IH Gliem, M Birtel, J Muller, PL Mangold, E Bolz, H Issa, PC The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 |
| title | The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 |
| title_full | The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 |
| title_fullStr | The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 |
| title_full_unstemmed | The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 |
| title_short | The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 |
| title_sort | retinal phenotype associated with the frequent synonymous c 783g a mutation in cdhr1 |
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