Variants in <i>BRWD3</i> associated with X‐linked partial epilepsy without intellectual disability-Reference-Cited by-同舟云学术

Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability

Published:2022-12-13 Issue:2 Volume:29 Page:727-735
ISSN:1755-5930
Container-title:CNS Neuroscience & Therapeutics
language:en
Short-container-title:CNS Neurosci Ther

Author:

Tian Mao‐Qiang¹²^ORCID,Liu Xiao‐Rong¹,Lin Si‐Mei¹,Wang Jie¹,Luo Sheng¹,Gao Liang‐Di¹,Chen Xiao‐Bin³,Liang Xiao‐Yu¹,Liu Zhi‐Gang⁴,He Na¹,Yi Yong‐Hong¹,Liao Wei‐Ping¹^ORCID,

Affiliation:

1. Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China Guangzhou China

2. Department of Pediatrics Affiliated Hospital of Zunyi Medical University Zunyi China

3. Department of Pediatrics The 900th Hospital of Joint Logistic Support Force Fuzhou China

4. Department of Pediatrics, Affiliated Foshan Maternity & Child Healthcare Hospital Southern Medical University Foshan China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

Pharmacology (medical),Physiology (medical),Psychiatry and Mental health,Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cns.14057

Reference37 articles.

1. Mutations in the BRWD3 Gene Cause X-Linked Mental Retardation Associated with Macrocephaly

2. Histone H3.3 maintains genome integrity during mammalian development

3. Diversity of WD-Repeat proteins

4. Identification of JAK/STAT signalling components by genome-wide RNA interference

5. Evidence for a non-canonical JAK/STAT signaling pathway in the synthesis of the brain’s major ion channels and neurotransmitter receptors

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