Bettina C. Thomas

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PURPOSE To elucidate the basis of the autosomal dominant congenital nuclear cataracts caused by the connexin50 mutant, CX50R23T, by determining its cellular distribution and functional behavior and the consequences of substituting other amino acids for arginine-23. METHODS Connexin50 (CX50) mutants were generated by PCR and transfected into HeLa or N2a(More)
PURPOSE The purpose of this study was to describe the visual prognosis as well as the frequency and clinical severity of central nervous system involvement in all acute posterior multifocal placoid pigment epitheliopathy (APMPPE) patients of one centre. METHODS A retrospective database review of all patients and a prospective clinical, ophthalmological(More)
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