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Carnitine transporter defect due to a novel mutation in theSLC22A5gene presenting with peripheral neuropathy

✍ Scribed by N. Makhseed; H.D. Vallance; M. Potter; P.J. Waters; L.T.K. Wong; Y. Lillquist; M. Pasquali; C. Amat di San Filippo; N. Longo

No coin nor oath required. For personal study only.

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