Hereditary macular diseases. [Int Ophthalmol Clin. 1999] - PubMed

A family with crystalline retinopathy demonstrating an autosomal dominant inheritance pattern. [Retina. 1999]
A family with crystalline retinopathy demonstrating an autosomal dominant inheritance pattern.
Miyauchi O, Murayama K, Adachi-Usami E. Retina. 1999; 19(6):573-4.
Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis. [Hum Genet. 1999]
Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis.
Hiraoka M, Trese MT, Shastry BS. Hum Genet. 1999 Jun; 104(6):526-7.
Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy. [Invest Ophthalmol Vis Sci. 2009]
Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy.
Boonstra FN, van Nouhuys CE, Schuil J, de Wijs IJ, van der Donk KP, Nikopoulos K, Mukhopadhyay A, Scheffer H, Tilanus MA, Cremers FP, et al. Invest Ophthalmol Vis Sci. 2009 Sep; 50(9):4379-85. Epub 2009 Mar 25.
Review The consortium project to treat RPE65 deficiency in humans. [Retina. 2005]
Review The consortium project to treat RPE65 deficiency in humans.
Hauswirth WW. Retina. 2005 Dec; 25(8 Suppl):S60.
Review The role of RPE65 in inherited retinal diseases. [Retina. 2005]
Review The role of RPE65 in inherited retinal diseases.
Bok D. Retina. 2005 Dec; 25(8 Suppl):S61-S62.

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Hereditary macular diseases.
Hereditary macular diseases.
Int Ophthalmol Clin. 1999 Fall ;39(4):83-115.

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