Case Report: Autofluorescence Imaging and Phenotypic Variance in a Sibling Pair with Early-Onset Retinal Dystrophy Due to Defective CRB1 Function

Author： Tosi Joaquin   Tsui Ilene   Lima Luiz   Wang Nan-Kai   Tsang Stephen  

Publisher： Informa Healthcare

ISSN： 0271-3683

Source： Current Eye Research, Vol.34, Iss.5, 2009-05, pp. : 395-400

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Retinal Dystrophy In The Oculo-auricular Syndrome Due to HMX1 Mutation

By Vaclavik V.   Schorderet D. F.   Borruat F-X.   Munier F. L.  

Ophthalmic Genetics, Vol. 32, Iss. 2, 2011-06 ,pp. : 114-117

Informa Healthcare

Access to resources Recommend Favorite

Retinal function in Bothnia dystrophy. An electrophysiological study

By Burstedt M.S.I.   Sandgren O.   Golovleva I.   Wachtmeister L.  

Vision Research, Vol. 43, Iss. 24, 2003-11 ,pp. : 2559-2571

Elsevier

Access to resources Recommend Favorite

Fundus Autofluorescence, Optical Coherence Tomography and Visual Acuity in Adult-Onset Foveomacular Dystrophy

By  

Ophthalmologica, Vol. 222, Iss. 4, 2008-05 ,pp. : 240-244

Karger

Access to resources Recommend Favorite

Mapping of retinal function in Best macular dystrophy using multifocal electroretinography

By Scholl H.P.N.   Schuster A.M.   Vonthein R.   Zrenner E.  

Vision Research, Vol. 42, Iss. 8, 2002-04 ,pp. : 1053-1061

Elsevier

Access to resources Recommend Favorite

Best Macular Dystrophy in a Nigerian: A Case Report

By  

Case Reports in Ophthalmology, Vol. 3, Iss. 2, 2012-06 ,pp. : 205-208

Karger

Access to resources Recommend Favorite