Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q-Reference-Cited by-同舟云学术

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Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q

Published:1997-07-01 Issue:1 Volume:63 Page:40-45
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Notelet L,Chapon F,Khoury S,Vahedi K,Chodkiewicz J P,Courtheoux P,Iba-Zizen M T,Cabanis E A,Lechevalier B,Tournier-Lasserve E,Houtteville J P

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Amplification of protease-activated receptors signaling in sporadic cerebral cavernous malformation endothelial cells;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2023-06

2. Editome landscape of CCM-derived endothelial cells;RNA Biology;2022-06-30

3. Whole-exome sequencing of Finnish patients with vascular cognitive impairment;European Journal of Human Genetics;2020-12-02

4. CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan;Scientific Reports;2019-08-27

5. Cerebrovascular disorders associated with genetic lesions;Cellular and Molecular Life Sciences;2018-10-16

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