Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1

By Wittströöm Elisabeth   Ekvall Sara   Schatz Patrik   Bondeson Marie-Louise   Ponjavic Vesna   Andrééasson Sten  

Ophthalmic Genetics, Vol. 32, Iss. 2, 2011-06 ,pp. : 83-96

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Anterior Segment Abnormalities and Angle-Closure Glaucoma in a Family with a Mutation in the BEST1 Gene and Best Vitelliform Macular Dystrophy

By Wittström Elisabeth   Ponjavic Vesna   Bondeson Marie-Louise   Andréasson Sten  

Ophthalmic Genetics, Vol. 32, Iss. 4, 2011-11 ,pp. : 217-227

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Expansion of the Clinical Ocular Spectrum of Wolfram Syndrome in a Family Carrying a Novel WFS1 Gene Deletion

By Chacón-Camacho Oscar   Arce-Gonzalez Rocio   Granillo-Alvarez Mariella   Flores-Limas Sanjuanita   Ramírez Magdalena   Zenteno Juan C.  

Ophthalmic Genetics, Vol. 34, Iss. 4, 2013-12 ,pp. : 243-248

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Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene

By Liskova Petra   Filipec Martin   Merjava Stanislava   Jirsova Katerina   Tuft Stephen J.  

Ophthalmic Genetics, Vol. 31, Iss. 4, 2010-12 ,pp. : 230-234

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Screening for NDP Mutations in 44 Unrelated Patients with Familial Exudative Vitreoretinopathy or Norrie Disease

By Yang Huiqin   Li Shiqiang   Xiao Xueshan   Guo Xiangming   Zhang Qingjiong  

Current Eye Research, Vol. 37, Iss. 8, 2012-08 ,pp. : 726-729

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