[cite web | title = Entrez Gene: MFRP membrane frizzled-related protein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=83552| accessdate = ] ] PBB_Summary
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References
Further reading
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*cite journal | author=Metlapally R, Li YJ, Tran-Viet KN, "et al." |title=Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia. |journal=Mol. Vis. |volume=14 |issue= |pages= 387-93 |year= |pmid= 18334955 |doi=
*cite journal | author=Ayala-Ramirez R, Graue-Wiechers F, Robredo V, "et al." |title=A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation. |journal=Mol. Vis. |volume=12 |issue= |pages= 1483-9 |year= 2007 |pmid= 17167404 |doi=
*cite journal | author=Yang L, Yamasaki K, Shirakata Y, "et al." |title=Bone morphogenetic protein-2 modulates Wnt and frizzled expression and enhances the canonical pathway of Wnt signaling in normal keratinocytes. |journal=J. Dermatol. Sci. |volume=42 |issue= 2 |pages= 111-9 |year= 2006 |pmid= 16442268 |doi= 10.1016/j.jdermsci.2005.12.011
*cite journal | author=Pauer GJ, Xi Q, Zhang K, "et al." |title=Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations. |journal=Ophthalmic Genet. |volume=26 |issue= 4 |pages= 157-61 |year= 2006 |pmid= 16352475 |doi= 10.1080/13816810500374425
*cite journal | author=Mandal MN, Heckenlively JR, Burch T, "et al." |title=Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform. |journal=Invest. Ophthalmol. Vis. Sci. |volume=46 |issue= 9 |pages= 3355-62 |year= 2005 |pmid= 16123440 |doi= 10.1167/iovs.05-0007
*cite journal | author=Sundin OH, Leppert GS, Silva ED, "et al." |title=Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 27 |pages= 9553-8 |year= 2005 |pmid= 15976030 |doi= 10.1073/pnas.0501451102
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Hayward C, Shu X, Cideciyan AV, "et al." |title=Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration. |journal=Hum. Mol. Genet. |volume=12 |issue= 20 |pages= 2657-67 |year= 2004 |pmid= 12944416 |doi= 10.1093/hmg/ddg289
*cite journal | author=Katoh M |title=Molecular cloning and characterization of MFRP, a novel gene encoding a membrane-type Frizzled-related protein. |journal=Biochem. Biophys. Res. Commun. |volume=282 |issue= 1 |pages= 116-23 |year= 2001 |pmid= 11263980 |doi= 10.1006/bbrc.2001.4551
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