Search Results - Hussaarts-Odijk, L.M.

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    Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency

    Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency by Vaz, F.M., Scholte, H.R., Ruiter, J., Hussaarts-Odijk, L.M., Rodrigues Pereira, R., Schweitzer, S., de Klerk, J.B.C., Waterham, H.R., Wanders, R.J.A.

    Published in Human genetics
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