9 research outputs found

    CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR

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    Clinical case of a patient with family hypercholesterolemia caused by mutation c.1859G>C (p.W620S) in the gene of human low density lipoproteins receptor

    Cephalopods in the marine ecosystems of the Paleozoic

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    Application of Extraction Methods for the Determin of Small Amounts of Metals

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    The electrophysics of a nerve fiber

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