Investigations on the Inheritance of Nemaline Myopathy
Author:
Publisher
American Medical Association (AMA)
Subject
Neurology (clinical),Arts and Humanities (miscellaneous)
Cited by 48 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. Congenital myopathies;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023
2. Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb;Acta Neuropathologica Communications;2020-02-17
3. Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy;Human Molecular Genetics;2015-06-29
4. Congenital Muscular Dystrophies and Congenital Myopathies;CONTINUUM: Lifelong Learning in Neurology;2013-12
5. Distinct Underlying Mechanisms of Limb and Respiratory Muscle Fiber Weaknesses in Nemaline Myopathy;Journal of Neuropathology & Experimental Neurology;2013-06
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