The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1

Մատենագիտական մանրամասներ
Հիմնական հեղինակներ: Yusuf, IH, Gliem, M, Birtel, J, Muller, PL, Mangold, E, Bolz, H, Issa, PC
Ձևաչափ: Conference item
Լեզու:English
Հրապարակվել է: Association for Research in Vision and Ophthalmology 2018
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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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