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Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality

While the outcomes of these bellwether trials are not binding on other claims, they could help the parties reach a GLP-1 settlement agreement that would avoid the need for each individual case to be sent back to its originating district for costly individual trials in the future

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Key features and benefits: - Contains hyaluronic acid to lock in moisture and enhance skin hydration treatment

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