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

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

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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

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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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