<scp> <i>CELSR1</i> </scp> variants are associated with partial epilepsy of childhood-Reference-Cited by-同舟云学术

CELSR1 variants are associated with partial epilepsy of childhood

Published:2022-08-12 Issue:7-8 Volume:189 Page:247-256
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:American J of Med Genetics Pt B

Author:

Chen Zheng¹²³,Luo Sheng¹²,Liu Zhi‐Gang⁴,Deng Yan‐Chun⁵,He Su‐Li⁶,Liu Xiao‐Rong¹²,Yi Yong‐Hong¹²,Wang Jie¹²,Gao Liang‐Di¹²,Li Bing‐Mei¹²,Wu Zhi‐Jun⁷,Ye Zi‐Long¹²,Liang De‐Hai¹²,Bian Wen‐Jun¹²,Liao Wei‐Ping¹²^ORCID,

Affiliation:

1. Institute of Neuroscience, Department of Neurology The Second Affiliated Hospital of Guangzhou Medical University Guangzhou China

2. Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province The Ministry of Education of China Guangzhou China

3. Department of Pediatrics The First Affiliated Hospital of Zhengzhou University Zhengzhou China

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

5. Department of Neurology, Xijing Hospital The Fourth Military Medical University Xi'an China

6. Department of Pediatrics Shantou Chaonan Minsheng Hospital Shantou China

7. Department of Neurology Second Hospital of Lanzhou University, Lanzhou University Lanzhou China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32916

Reference47 articles.

1. A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome

2. PRICKLE2 revisited—further evidence implicating PRICKLE2 in neurodevelopmental disorders

3. Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders

4. Genetic models of focal epilepsies

5. Celsr1–3 Cadherins in PCP and Brain Development

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