Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa

By Zhao Kanxing   Xiong Shihong   Wang Li   Wang Lejin   Cui Yun   Wang Qing  

Ophthalmic Genetics, Vol. 22, Iss. 3, 2001-09 ,pp. : 155-162

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Homozygous and heterozygous Gly-188-Arg mutation of the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa

By Reig Carlos   Trujillo M. José   Martinez-Gimeno Maria   Garcia-Sandoval Blanca   Calvo M. Teresa   Ayuso Carmen   Carballo Miguel  

Ophthalmic Genetics, Vol. 21, Iss. 2, 2000-06 ,pp. : 79-87

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Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa

By Souied E.H.   Benlian P.   Rozet J.-M.   Gerber S.   Lagarde J.-P.   Coscas G.   Soubrane G.   Duffier J.-L.   Munnich A.   Kaplan J.  

Vision Research, Vol. 38, Iss. 24, 1998-12 ,pp. : 3829-3831

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Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)

By van Lith-Verhoeven J.J.C.   van der Velde-Visser S.D.   Sohocki M.M.   Deutman A.F.   Brink H.M.A.   Cremers F.P.M.   Hoyng C.B.  

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Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N

By Tsui Irena   Chou Chai Lin   Palmer Neeco   Lin Chyuan-Sheng   Tsang Stephen  

Current Eye Research, Vol. 33, Iss. 11-12, 2008-11 ,pp. : 1014-1022

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