Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene

By Ponjavic Vesna   Eksandh Louise   Andréasson Sten   Sjöström Kerstin   Bakall B.   Ingvast S.   Wadelius Claes   Ehinger Berndt  

Ophthalmic Genetics, Vol. 20, Iss. 4, 1999-12 ,pp. : 251-257

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Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy

By Marchant D.   Gogat K.   Dureau P.   Sainton K.   Sternberg C.   Gadin S.   Dollfus H.   Brasseur G.   Hache J.C.   Dumur V.   Puech V.   Munier F.L.   Schorderet D.F.   Marsac C.   Menasche M.   Dufier J.L.   Abitbol M.  

Ophthalmic Genetics, Vol. 23, Iss. 3, 2002-09 ,pp. : 167-174

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Variant Phenotype of Best Vitelliform Macular Dystrophy Associated with Compound Heterozygous Mutations in VMD2

By Schatz Patrik   Klar Joakim   Andréasson Sten   Ponjavic Vesna   Dahl Niklas  

Ophthalmic Genetics, Vol. 27, Iss. 2, 2006-07 ,pp. : 51-56

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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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Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene

By Eksandh Louise   Bakall Benjamin   Bauer Birgitta   Wadelius Claes   Andréasson Sten  

Ophthalmic Genetics, Vol. 22, Iss. 2, 2001-06 ,pp. : 107-115

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