| 1 | MFRP, MPRF
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| A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.
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| Mukhopadhyay R, Sergouniotis PI, Mackay DS, Day AC, Wright G, Devery S, Leroy BP, Robson AG, Holder GE, Li Z, Webster AR.
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| Mol Vis 16:540-8.PMID: 20361016 2010
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| 2 | MFRP, MPRF, NNO2
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| Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex.
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| Zenteno JC, Buentello-Volante B, Quiroz-González MA, Quiroz-Reyes MA.
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| Mol Vis 15:1794-8.PMID: 19753314 2009
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| 3 | MFRP
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| Evaluation of MFRP as a candidate gene for high hyperopia.
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| Wang P, Yang Z, Li S, Xiao X, Guo X, Zhang Q.
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| Mol Vis 15:181-6. Epub 2009 Jan 23.PMID: 19169412 2009
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| 4 | MFRP, MPRF
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| A novel mutation confirms MFRP as the gene causing the syndrome of nanophthalmos-renititis pigmentosa-foveoschisis-optic disk drusen.
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| Crespí J, Buil JA, Bassaganyas F, Vela-Segarra JI, Díaz-Cascajosa J, Ayala-Ramírez R, Zenteno JC.
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| Am J Ophthalmol 146(2):323-328. Epub 2008 Jun 13.PMID: 18554571 2008
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| 5 | MFRP, MPRF
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| A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation.
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| Ayala-Ramirez R, Graue-Wiechers F, Robredo V, Amato-Almanza M, Horta-Diez I, Zenteno JC.
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| Mol Vis 12:1483-9. 2006
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| 6 | NNO2, MFRP, NLRX1, TMEM25
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| Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.
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| Sundin OH, Leppert GS, Silva ED, Yang JM, Dharmaraj S, Maumenee IH, Santos LC, Parsa CF, Traboulsi EI, Broman KW, Dibernardo C, Sunness JS, Toy J, Weinberg EM.
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| Proc Natl Acad Sci U S A 102(27):9553-9558. Epub 2005 Jun 23. 2005
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| 7 | TTC12, DIXDC1, MFRP, RNF26, CLDN24
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| Identification and characterization of TPARM gene in silico.
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| Katoh M, Katoh M.
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| Int J Oncol 23(4):1213-7. 2003
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| 8 | MFRP
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| Molecular cloning and characterization of MFRP, a novel gene encoding amembrane-type Frizzled-related protein.
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| Katoh M.
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| Biochem Biophys Res Commun 282(1):116-23. 2001
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