CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan-Reference-Cited by-同舟云学术

CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan

Published:2019-08-27 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Chang Chun-Wei^ORCID,Hsu Peng-Wei,Wei Kuo-Chen,Chang Chia-Wen,Fung Hon-Chung,Hsih Mo-Song,Hsu Wen-Chuin,Ro Long-Sun,Chang Chen-Nen,Wang Jiun-Jie,Wu Yih-Ru,Chen Sien-Tsong

Funder

Chang Gung Memorial Hospital, Linkou

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-48448-y.pdf

Reference30 articles.

1. Robinson, J. R., Awad, I. A. & Little, J. R. Natural history of the cavernous angioma. J Neurosurg 75, 709–714 (1991).

2. Gunel, M. et al. Genetic heterogeneity of inherited cerebral cavernous malformation. Neurosurgery 38, 1265–1271 (1996).

3. Notelet, L. et al. Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q. J Neurol Neurosurg Psychiatry 63, 40–45 (1997).

4. Dupre, N. et al. Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation. Can J Neurol Sci 30, 122–128 (2003).

5. Bergametti, F. et al. Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations. Am J Hum Genet 76, 42–51 (2005).

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