Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2-Reference-Cited by-同舟云学术

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Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2

Published:2006-06-01 Issue:6 Volume:13 Page:339-351
ISSN:1052-2166
Container-title:Gene Expression
language:en
Short-container-title:ge

Author:

BOTTA ANNALISA,VALLO LAURA,RINALDI FABRIZIO,BONIFAZI EMANUELA,AMATI FRANCESCA,BIANCOLELLA MICHELA,GAMBARDELLA STEFANO,MANCINELLI ENZO,ANGELINI CORRADO,MEOLA GIOVANNI,NOVELLI AND GIUSEPPE

Publisher

Cognizant, LLC

Subject

Genetics,Molecular Biology

Cited by 34 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. Muscular Dystrophy: Mutations in the Dystrophin Gene;Mechanism and Genetic Susceptibility of Neurological Disorders;2024

2. Exome sequencing identifies a novel pathogenic CLCN1 mutation in an Iranian family with Myotonia Congenita: A case report;Human Gene;2022-12

3. The polyG diseases: a new disease entity;Acta Neuropathologica Communications;2022-05-31

4. Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1;International Journal of Molecular Sciences;2021-08-10

5. TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease;Progress in Retinal and Eye Research;2021-03

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