Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy-Reference-Cited by-同舟云学术

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Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy

Published:2017-10 Issue: Volume:Volume 13 Page:2631-2636
ISSN:1178-2021
Container-title:Neuropsychiatric Disease and Treatment
language:en
Short-container-title:NDT

Author:

Lv Yudan,Wang Zan,Liu Chang,Cui Li

Publisher

Informa UK Limited

Cited by 19 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. A Review of the CACNA Gene Family: Its Role in Neurological Disorders;Diseases;2024-05-05

2. Progressive Myoclonus Epilepsy: A Scoping Review of Diagnostic, Phenotypic and Therapeutic Advances;Genes;2024-01-27

3. Screening of the Key Genes and Signaling Pathways for Schizophrenia Using Bioinformatics and Next Generation Sequencing Data Analysis;2023-10-29

4. The genotype–phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews;Frontiers in Molecular Neuroscience;2023-07-24

5. Biallelic CACNA1A variants: Review of literature and report of a child with drug‐resistant epilepsy and developmental delay;American Journal of Medical Genetics Part A;2022-09-05

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