Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: Biochemical signs of combined sphingolipidoses
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A. Poulos | M. Popp | T. Grisar | W. Roggendorf | K. Harzer | B. Kustermann-Kuhn | B. Paton | Alf Poulos | Barbara C. Paton