Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice.

A. Kennan; A. Aherne; A. Palfi; M. Humphries; A. McKee; Alan Stitt; David Simpson; K. Demtroder; T. Orntoft; C. Ayuso; P.F. Kenna; G.J. Farrar; P. Humphries

doi:10.1093/hmg/11.5.547

Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice.

A. Kennan, A. Aherne, A. Palfi, M. Humphries, A. McKee, Alan Stitt, David Simpson, K. Demtroder, T. Orntoft, C. Ayuso, P.F. Kenna, G.J. Farrar, P. Humphries

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150 Citations (Scopus)

Original language	English
Pages (from-to)	547-558
Number of pages	12
Journal	Human Molecular Genetics
Volume	11(5)
Issue number	5
DOIs	https://doi.org/10.1093/hmg/11.5.547
Publication status	Published - 01 Jan 2002

ASJC Scopus subject areas

Genetics

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Kennan, A., Aherne, A., Palfi, A., Humphries, M., McKee, A., Stitt, A., Simpson, D., Demtroder, K., Orntoft, T., Ayuso, C., Kenna, P. F., Farrar, G. J., & Humphries, P. (2002). Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice. Human Molecular Genetics, 11(5)(5), 547-558. https://doi.org/10.1093/hmg/11.5.547

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author = "A. Kennan and A. Aherne and A. Palfi and M. Humphries and A. McKee and Alan Stitt and David Simpson and K. Demtroder and T. Orntoft and C. Ayuso and P.F. Kenna and G.J. Farrar and P. Humphries",

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Kennan, A, Aherne, A, Palfi, A, Humphries, M, McKee, A, Stitt, A , Simpson, D, Demtroder, K, Orntoft, T, Ayuso, C, Kenna, PF, Farrar, GJ & Humphries, P 2002, 'Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice.', Human Molecular Genetics, vol. 11(5), no. 5, pp. 547-558. https://doi.org/10.1093/hmg/11.5.547

Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice. / Kennan, A.; Aherne, A.; Palfi, A. et al.
In: Human Molecular Genetics, Vol. 11(5), No. 5, 01.01.2002, p. 547-558.

Research output: Contribution to journal › Article › peer-review

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Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice.

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