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Ueda K, Serajee F, Huq AM. A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions. J Clin Neurol. 2017;13(3):300-302doi: 10.3988/jcn.2017.13.3.300.
Ueda, K., Serajee, F., & Huq, A. M. (2017). A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions. Journal of clinical neurology (Seoul, Korea), 13(3), 300-302. https://doi.org/10.3988/jcn.2017.13.3.300
Ueda, Keisuke, et al. "A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions." Journal of clinical neurology (Seoul, Korea) vol. 13,3 (2017): 300-302. doi: https://doi.org/10.3988/jcn.2017.13.3.300
Ueda K, Serajee F, Huq AM. A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions. J Clin Neurol. 2017 Jul;13(3):300-302. doi: 10.3988/jcn.2017.13.3.300. Epub 2017 Apr 06. PMID: 28516742; PMCID: PMC5532330.
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J Clin Neurol. 2017 Jul;13(3):300-302. doi: 10.3988/jcn.2017.13.3.300. Epub 2017 Apr 06.

A Mutation in the ACTA1 gene Manifesting Nemaline Myopathy with Central Nervous System Lesions.

Journal of clinical neurology (Seoul, Korea)

Keisuke Ueda, Fatema Serajee, Ahm M Huq

Affiliations

  1. Division of Child Neurology, Children's Hospital of Michigan, Wayne State University School of Medicine, Detroit, MI, USA. [email protected].
  2. Division of Child Neurology, Children's Hospital of Michigan, Wayne State University School of Medicine, Detroit, MI, USA.

PMID: 28516742 PMCID: PMC5532330 DOI: 10.3988/jcn.2017.13.3.300

[No abstract available.]

Conflict of interest statement

The authors have no financial conflicts of interest.

References

  1. Ann Neurol. 2001 Sep;50(3):312-20 - PubMed
  2. J Cell Sci. 2004 Jul 1;117(Pt 15):3367-77 - PubMed
  3. Semin Pediatr Neurol. 2011 Dec;18(4):230-8 - PubMed
  4. Neuromuscul Disord. 1998 Feb;8(1):53-6 - PubMed

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