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    A mild skeletal phenotype with overlapping features of Miller syndrome and functional characterisation of two new variants of human dihydroorotate dehydrogenase

    A mild skeletal phenotype with overlapping features of Miller syndrome and functional characterisation of two new variants of human dihydroorotate dehydrogenase von Mero, Inger-Lise, Orozco Rodriguez, Juan Manuel, Bjørgo, Kathrine, Hankin, Renee Alexandra, Krupinska, Ewa, Kulseth, Mari Ann, Rossow, Marvin Anthony, Knecht, Wolfgang

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