Mutations of the slow muscle -tropomyosin gene, TPM3, are a rare cause of nemaline myopathy-Reference-Cited by-同舟云学术

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Mutations of the slow muscle -tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

Published:2002-08-27 Issue:4 Volume:59 Page:613-617
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Wattanasirichaigoon D.,Swoboda K. J.,Takada F.,Tong H.-Q.,Lip V.,Iannaccone S. T.,Wallgren-Pettersson C.,Laing N. G.,Beggs A. H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 78 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. Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy;Skeletal Muscle;2023-11-07

2. Novel Compound Heterozygous Splice-Site Variants in TPM3 Revealed by RNA Sequencing in a Patient with an Unusual Form of Nemaline Myopathy: A Case Report;Journal of Neuromuscular Diseases;2023-09-08

3. Novel autosomal dominant TPM3 mutation causes a combined congenital fibre type disproportion-cap disease histological pattern;Neuromuscular Disorders;2022-08

4. Transcript-Based Diagnosis and Expanded Phenotype of an Intronic Mutation in TPM3 Myopathy;Molecular Diagnosis & Therapy;2022-07-07

5. Importance of electromyography in children;Pediatru.ro;2022

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