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Cone Structure in Patients With Usher Syndrome Type III and Mutations in the Clarin 1 Gene

OBJECTIVE: To study macular structure and function in patients with Usher syndrome type III (USH3) caused by mutations in the Clarin 1 gene (CLRN1). METHODS: High-resolution macular images were obtained by adaptive optics scanning laser ophthalmoscopy and spectral domain optical coherence tomography...

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書誌詳細
出版年:JAMA Ophthalmol
主要な著者: Ratnam, Kavitha, Västinsalo, Hanna, Roorda, Austin, Sankila, Eeva-Marja K., Duncan, Jacque L.
フォーマット: Artigo
言語:Inglês
出版事項: 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4482614/
https://ncbi.nlm.nih.gov/pubmed/22964989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/2013.jamaophthalmol.2
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