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Muscle tissue becomes more vulnerable to breakdown
Skin that was stretched over a larger body mass needs time and biological support to remodel
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doi: 10.1080/00325481.2021.2002616 4 KunutsorSKSeiduS
Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)
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