A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 ( RP11) von Vithana, Eranga N., Abu-Safieh, Leen, Allen, Maxine J., Carey, Alisoun, Papaioannou, Myrto, Chakarova, Christina, Al-Maghtheh, Mai, Ebenezer, Neil D., Willis, Catherine, Moore, Anthony T., Bird, Alan C., Hunt, David M., Bhattacharya, Shomi S.

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Rhodopsin mutations in autosomal dominant retinitis pigmentosa von Al-Maghtheh, Mai, Gregory, Cheryl, Inglehearn, Chris, Hardcastle, Alison, Bhattacharya, Shomi

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Evidence for interaction between human PRUNE and nm23-H1 NDPKinase von REYMOND, A, VOLORIO, S, MERLA, G, AL-MAGHTHEH, M, ZUFFARDI, O, BULFONE, A, BALLABIO, A, ZOLLO, M

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Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19 von Al-Maghtheh, Mai, Inglehearn, Chris F., Jeffrey, T. Keen, Evans, Kevin, Moore, Anthony T., Jay, Marcelle, Bird, Alan C., Bhattacharya, Shomi S.

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Two new rhodopsin transversion mutations (L40R; M216K) in families with autosomal dominant retinitis pigmentosa von Al-Maghtheh, Mai, Inglehearn, Chris, Lunt, Peter, Jay, Marcelle, Bird, Alan, Bhattacharya, Shomi

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Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11), and association with a unique bimodal expressivity phenotype von AL-MAGHTHEH, M, VITHANA, E, TARTTELIN, E, JAY, M, EVANS, K, MOORE, T, BHATTACHARYA, S, INGLEHEARN, C. F

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Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p(RP9) von INGLEHEARN, C. F, KEEN, T. J, MAI AL-MAGHTHEH, GREGORY, C. Y, JAY, M. R, MOORE, A. T, BIRD, A. C, BHATTACHARYA, S. S

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Segregation of a PRKCG Mutation in Two RP11 Families von Al-Maghtheh, Mai, Vithana, Eranga N., Inglehearn, Chris F., Moore, Tony, Bird, Alan C., Bhattacharya, Shomi S.

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A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity von Inglehearn, C F, Tarttelin, E E, Plant, C, Peacock, R E, al-Maghtheh, M, Vithana, E, Bird, A C, Bhattacharya, S S

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Identification of a sicth locus for autosomal dominant retinitis pigmentosa on chromosome 19 von MAI AL-MAGHTHEH, INGELHEARN, C. F, KEEN, T. J, EVANS, K, MOORE, A. T, JAY, M, BIRD, A. C, BHATTACHARYA, S. S

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