The predictive value of models of neuromuscular disorders to potentiate clinical translation

Author:

van Putten Maaike1ORCID

Affiliation:

1. Leiden University Medical Center , Department of Human Genetics, 2333 ZC Leiden , The Netherlands

Abstract

ABSTRACT Neuromuscular disorders (NMDs) are a heterogenous group of rare inherited diseases that compromise the function of peripheral nerves and/or muscles. With limited treatment options available, there is a growing need to design effective preclinical studies that can lead to greater success in clinical trials for novel therapeutics. Here, I discuss recent advances in modelling NMDs to improve preclinical studies as well as two articles from this issue that work in parallel to enable a deeper understanding of a particularly rare NMD, known as X-linked myotubular myopathy.

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

Cited by 3 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. Supporting the translation of multiscale research in rare disease;Disease Models & Mechanisms;2023-09-01

2. Impactful disease research: a DMM year in review;Disease Models & Mechanisms;2023-01-01

3. Sharing resources to advance translational research;Disease Models & Mechanisms;2022-10-01

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