Mutation Analysis of the VMD2 Gene in Thai Families with Best Macular Dystrophy

By Atchaneeyasakul La-ongsri   Jinda Worapoj   Sakolsatayadorn Natta   Trinavarat Adisak   Ruangvoravate Ngamkae   Thanasombatskul Nualanong   Thongnoppakhun Wanna   Limwongse Chanin  

Ophthalmic Genetics, Vol. 29, Iss. 3, 2008-09 ,pp. : 139-144

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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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1147 del A mutation in the arrestin gene in Japanese patients with Oguchi disease

By Yamada Tetsuya   Matsumoto Masayuki   Kadoi Chiharu   Nagaki Yasunori   Hayasaka Yoriko   Hayasaka Seiji  

Ophthalmic Genetics, Vol. 20, Iss. 2, 1999-06 ,pp. : 117-120

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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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