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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OCT findings in young asymptomatic subjects carrying familial BEST1 gene mutations

By Chacon-Camacho Oscar F.   Camarillo-Blancarte Leyla   Zenteno Juan C.  

Ophthalmic Genetics, Vol. 32, Iss. 1, 2011-03 ,pp. : 24-30

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Novel BEST1 Mutations and Special Clinical Features of Best Vitelliform Macular Dystrophy

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Ophthalmic Research, Vol. 56, Iss. 4, 2016-04 ,pp. : 178-185

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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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