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1, 2 IGF-1R and Thyroid Eye Disease IGF-1R plays a significant role in the pathogenesis of TED
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Others received no local medication: they were treated i.p
112 MeCP2 deletions or point mutations on the X chromosome in females manifest as Rett syndrome, a serious neurological disorder with autism-like symptoms
This matters in chronic inflammatory conditions where oxidative stress can worsen tissue damage
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