Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole‐exome sequencing-Reference-Cited by-同舟云学术

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Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole‐exome sequencing

Published:2022-11-07 Issue:12 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Xu Yan¹,Zhao Rui²,Wang Min²,Wang Xin‐hua¹,Wang Yi¹,Li Hao²,Ma Yang‐yang³,Wu Bing‐bing⁴,Zhou Yuan‐feng¹^ORCID

Affiliation:

1. Department of Neurology and Epilepsy Center Children's Hospital of Fudan University Shanghai China

2. Department of Neurosurgery Children's Hospital of Fudan University Shanghai China

3. Department of Pathology Children's Hospital of Fudan University Shanghai China

4. Center for Molecular Medicine Pediatrics Research Institute, Children's Hospital of Fudan University Shanghai China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2086

Reference24 articles.

1. Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy

2. Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial

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