Congenital myasthenic syndrome in China: genetic and myopathological characterization-Reference-Cited by-同舟云学术

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Congenital myasthenic syndrome in China: genetic and myopathological characterization

Published:2021-03-23 Issue:4 Volume:8 Page:898-907
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann. Clin. Transl. Neurol.

Author:

Zhao Yawen¹^ORCID,Li Ying²,Bian Yang³,Yao Sheng³,Liu Penju²,Yu Meng¹^ORCID,Zhang Wei¹,Wang Zhaoxia¹^ORCID,Yuan Yun¹

Affiliation:

1. Department of Neurology Peking University First Hospital Beijing China

2. Department of Neurology Capital Medical University Affiliated Anzhen Hospital Chaoyang‐qu China

3. Department of Neurology Sixth Medical Center of PLA General Hospital Beijing China

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51346

Reference36 articles.

1. Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment

2. Congenital Myasthenic Syndromes in 2018

3. Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

4. Molecular characterization of congenital myasthenic syndromes in Spain

5. Congenital myasthenic syndromes: Achievements and limitations of phenotype-guided gene-after-gene sequencing in diagnostic practice: A study of 680 patients

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1. Congenital myasthenic syndromes: increasingly complex;Current Opinion in Neurology;2024-07-25

2. Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort;Brain;2023-09-18

3. Pharmacological Treatments for Congenital Myasthenic Syndromes Caused by COLQ Mutations;Current Neuropharmacology;2023-07

4. COLQ-related congenital myasthenic syndrome: An integrative view;neurogenetics;2023-05-25

5. Mitochondrial Mutations Can Alter Neuromuscular Transmission in Congenital Myasthenic Syndrome and Mitochondrial Disease;International Journal of Molecular Sciences;2023-05-09

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