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pro vyhledávání: '"I. M. Speidel"'
Autor:
Georg F. Hoffmann, S. R. Scharfschwerdt, Yoon S. Shin, K. M. Gibson, S. U. Brendel, I. M. Speidel
Publikováno v:
Journal of Inherited Metabolic Disease. 15:738-746
Mevalonic aciduria due to mevalonate kinase deficiency, an inherited defect of cholesterol biosynthesis, has presented with clinical variability in 10 patients from 7 families. We sought to define a genetic basis for this heterogeneity by determining