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Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: Biochemical signs of combined sphingolipidoses
K. Harzer, B. C. Paton, A. Poulos, B. Kustermann-Kuhn, W. Roggendorf, T. Grisar, M. PoppVolume:
149
Language:
english
Pages:
9
DOI:
10.1007/bf02024331
Date:
October, 1989
File:
PDF, 2.68 MB
english, 1989