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ACTA1 gene

Known as: nemaline myopathy type 3, actin, alpha 1, skeletal muscle, ACTA1 
 
National Institutes of Health

Papers overview

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2019
2019
Tujuan penelitian ini untuk mengetahui hubungan status kontrol asma dengan kualitas hidup pada anak dengan asma bronkial di RSUD… Expand
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2019
2019
BackgroundHead and neck squamous cell carcinoma (HNSCC) is the six leading cancer by incidence worldwide. The 5-year survival… Expand
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2015
2015
IMPORTANCE New genomic strategies can now be applied to identify a diagnosis in patients and families with previously undiagnosed… Expand
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2015
2015
We present follow up data on the original case of 'zebra body myopathy' published by Lake and Wilson in 1975. Pathological… Expand
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2014
2014
A boy, who had shown muscle weakness and hypotonia from early childhood and fiber type disproportion (FTD) with no dystrophic… Expand
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2010
2010
The aim of the present study was to analyse the morphology of white skeletal muscle in males and females from the GH-transgenic… Expand
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2010
2010
Die zirkumskripte Sklerodermie ist eine autoimmunologische Erkrankung. Es wurden 398 Patienten mit einer zirkumskripten… Expand
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2009
2009
Penyakit asma awalnya merupakan penyakit genetik yang diturunkan dari orang tua yang karier pada anaknya. Namun, akhir-akhir ini… Expand
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2007
2007
OBJECTIVE Mutations in ACTA1 have been associated with a variety of changes in muscle histology that likely result from… Expand
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1995
1995
We present the molecular characterization of the asmA gene, whose product is involved in the assembly of outer membrane proteins… Expand
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