Nemaline Myopathy with Exclusively Intranuclear Rods and a Novel Mutation in ACTA1 (Q139H)-Reference-Cited by-同舟云学术

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Nemaline Myopathy with Exclusively Intranuclear Rods and a Novel Mutation in ACTA1 (Q139H)

Published:2007-12 Issue:6 Volume:38 Page:282-286
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Koy A.,Ilkovski B.,Laing N.,North K.,Weis J.,Neuen-Jacob E.,Mayatepek E.,Voit T.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2008-1065356.pdf

Cited by 15 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. Cofilin and Actin Dynamics: Multiple Modes of Regulation and Their Impacts in Neuronal Development and Degeneration;Cells;2021-10-12

2. Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy;Journal of Medical Genetics;2020-09-29

3. Skeletal Muscle Biopsy Evaluation;A Case-Based Guide to Neuromuscular Pathology;2019-10-25

4. Nemaline myopathies: a current view;Journal of Muscle Research and Cell Motility;2019-06

5. Diseases of the skeletal muscle;Handbook of Clinical Neurology;2018

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