Newly discovered COLQ gene mutation and its clinical features in patients with acetyl cholinesterase deficiency-Reference-Cited by-同舟云学术

Newly discovered COLQ gene mutation and its clinical features in patients with acetyl cholinesterase deficiency

Published:2018-09-12 Issue:3-4 Volume:17 Page:439-446
ISSN:1757-448X
Container-title:Journal of Integrative Neuroscience
language:
Short-container-title:JIN

Author:

Zhang Qing-Lin¹,Xu Ming-Jun¹,Wang Tian-Long²,Zhu Zi-Qiong¹,Lai Fancai³,Zheng Xiao-Chun⁴⁵

Affiliation:

1. Department of Anesthesiology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Postcode: 100026, China. E-mails: drlynn@163.com, snake650222@163.com, tuwenshao@sina.com

2. Department of Anesthesiology of Xuanwu Hospital, Capital Medical University, Postcode: 100053, China. E-mail: wtl5595@hotmail.com

3. Department of Thoracic Surgery, 1st Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China

4. Department of Anesthesiology of Provincial Clinical College, Fujian Medical University, Postcode: 350001, China

5. Department of Emergency, Fujian Provincial Hospital, Postcode: 350001, China. E-mail: 114118814@qq.com

Publisher

IOS Press

Subject

General Medicine,General Neuroscience

Reference9 articles.

1. M. Abitbol, C. Hitte, P. Bossé et al., A COLQ missense mutation in Sphynx and Devon Rex cats with congenital myasthenic syndrome, PLoS One 10(9) (2015), e0137019.

2. COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy;Gandolfi;Anim. Genet.,2015

3. Initial sequencing and analysis of the human genome;International Human Genome Sequencing Consortium;Nature,2000

4. Q.C. Liu, F. Chen, C.Y. Wu et al., CALCB splice region pathogenic variants leading to plasma cell neurotropic enrichment in type 1 autoimmune pancreatitis, Cell Death Dis. 8(2) (2017), e2591.

5. The polymorphism of acetyl-cholinesterase: Post-translational processing,quaternary associations and localization;Massoulie;Chen. Biol. Interact.,1999

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