[cite web | title = Entrez Gene: CCM2 cerebral cavernous malformation 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=83605| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Craig HD, Günel M, Cepeda O, "et al." |title=Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27. |journal=Hum. Mol. Genet. |volume=7 |issue= 12 |pages= 1851–8 |year= 1998 |pmid= 9811928 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Scherer SW, Cheung J, MacDonald JR, "et al." |title=Human chromosome 7: DNA sequence and biology. |journal=Science |volume=300 |issue= 5620 |pages= 767–72 |year= 2003 |pmid= 12690205 |doi= 10.1126/science.1083423
*cite journal | author=Dupré N, Verlaan DJ, Hand CK, "et al." |title=Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation. |journal=The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques |volume=30 |issue= 2 |pages= 122–8 |year= 2003 |pmid= 12774951 |doi=
*cite journal | author=Liquori CL, Berg MJ, Siegel AM, "et al." |title=Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations. |journal=Am. J. Hum. Genet. |volume=73 |issue= 6 |pages= 1459–64 |year= 2004 |pmid= 14624391 |doi=
*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=Denier C, Goutagny S, Labauge P, "et al." |title=Mutations within the MGC4607 gene cause cerebral cavernous malformations. |journal=Am. J. Hum. Genet. |volume=74 |issue= 2 |pages= 326–37 |year= 2004 |pmid= 14740320 |doi=
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Wan D, Gong Y, Qin W, "et al." |title=Large-scale cDNA transfection screening for genes related to cancer development and progression. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 44 |pages= 15724–9 |year= 2004 |pmid= 15498874 |doi= 10.1073/pnas.0404089101
*cite journal | author=Zawistowski JS, Stalheim L, Uhlik MT, "et al." |title=CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis. |journal=Hum. Mol. Genet. |volume=14 |issue= 17 |pages= 2521–31 |year= 2005 |pmid= 16037064 |doi= 10.1093/hmg/ddi256
*cite journal | author=Guclu B, Ozturk AK, Pricola KL, "et al." |title=Cerebral venous malformations have distinct genetic origin from cerebral cavernous malformations. |journal=Stroke |volume=36 |issue= 11 |pages= 2479–80 |year= 2006 |pmid= 16239636 |doi= 10.1161/01.STR.0000183616.99139.d3
*cite journal | author=Seker A, Pricola KL, Guclu B, "et al." |title=CCM2 expression parallels that of CCM1. |journal=Stroke |volume=37 |issue= 2 |pages= 518–23 |year= 2006 |pmid= 16373645 |doi= 10.1161/01.STR.0000198835.49387.25
*cite journal | author=Labauge P, Krivosic V, Denier C, "et al." |title=Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study. |journal=Arch. Ophthalmol. |volume=124 |issue= 6 |pages= 885–6 |year= 2006 |pmid= 16769843 |doi= 10.1001/archopht.124.6.885
*cite journal | author=Liquori CL, Berg MJ, Squitieri F, "et al." |title=Deletions in CCM2 are a common cause of cerebral cavernous malformations. |journal=Am. J. Hum. Genet. |volume=80 |issue= 1 |pages= 69–75 |year= 2007 |pmid= 17160895 |doi= 10.1086/510439
*cite journal | author=Zhang J, Rigamonti D, Dietz HC, Clatterbuck RE |title=Interaction between krit1 and malcavernin: implications for the pathogenesis of cerebral cavernous malformations. |journal=Neurosurgery |volume=60 |issue= 2 |pages= 353–9; discussion 359 |year= 2007 |pmid= 17290187 |doi= 10.1227/01.NEU.0000249268.11074.83
*cite journal | author=Gianfrancesco F, Cannella M, Martino T, "et al." |title=Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations. |journal=Am. J. Med. Genet. B Neuropsychiatr. Genet. |volume=144 |issue= 5 |pages= 691–5 |year= 2007 |pmid= 17440989 |doi= 10.1002/ajmg.b.30381
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