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Journal of Neurology
Published in: Journal of Neurology 12/2010

01-12-2010 | Letter to the Editors

Multiple cerebral cavernous malformations and a novel CCM3 germline deletion in a German family

Authors: Chi-un Choe, Florence Riant, Christian Gerloff, Elisabeth Tournier-Lasserve, Michael Orth

Published in: Journal of Neurology | Issue 12/2010

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Excerpt

Dear Sirs, …
Literature
1.
Craig HD, Gunel M, Cepeda O, Johnson EW, Ptacek L, Steinberg GK, Ogilvy CS, Berg MJ, Crawford SC, Scott RM, Steichen-Gersdorf E, Sabroe R, Kennedy CT, Mettler G, Beis MJ, Fryer A, Awad IA, Lifton RP (1998) Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15–13 and 3q25.2–27. Hum Mol Genet 7:1851–1858CrossRefPubMed
2.
Guclu B, Ozturk AK, Pricola KL, Bilguvar K, Shin D, O’Roak BJ, Gunel M (2005) Mutations in apoptosis-related gene, PDCD10, cause cerebral cavernous malformation 3. Neurosurgery 57:1008–1013CrossRefPubMed
3.
Labauge P, Denier C, Bergametti F, Tournier-Lasserve E (2007) Genetics of cavernous angiomas. Lancet Neurol 6:237–244CrossRefPubMed
4.
Liquori CL, Berg MJ, Squitieri F, Ottenbacher M, Sorlie M, Leedom TP, Cannella M, Maglione V, Ptacek L, Johnson EW, Marchuk DA (2006) Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus. Hum Mutat 27:118CrossRefPubMed
5.
Liquori CL, Penco S, Gault J, Leedom TP, Tassi L, Esposito T, Awad IA, Frati L, Johnson EW, Squitieri F, Marchuk DA, Gianfrancesco F (2008) Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts. Neurogenetics 9:25–31CrossRefPubMed
6.
Verlaan DJ, Roussel J, Laurent SB, Elger CE, Siegel AM, Rouleau GA (2005) CCM3 mutations are uncommon in cerebral cavernous malformations. Neurology 65:1982–1983CrossRefPubMed
Metadata
Title
Multiple cerebral cavernous malformations and a novel CCM3 germline deletion in a German family
Authors
Chi-un Choe
Florence Riant
Christian Gerloff
Elisabeth Tournier-Lasserve
Michael Orth
Publication date
01-12-2010
Publisher
Springer-Verlag
Published in
Journal of Neurology / Issue 12/2010
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-010-5648-7

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