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Detection of FLAD1 mutations and lipid storage myopathy in a 5-year-old boy: a case report study.

Seyed Ahmad HosseiniLayla ShojaieMousa Ghelichi-Ghojogh
Published in: Annals of medicine and surgery (2012) (2023)
gene is recommended in all people with multiple acyl-CoA dehydrogenase deficiency.
Keyphrases
  • fatty acid
  • late onset
  • copy number
  • gene expression
  • loop mediated isothermal amplification
  • transcription factor
  • replacement therapy
  • duchenne muscular dystrophy
  • muscular dystrophy