(Q28186070)
Statements
Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene (English)
D. Schnabel
M. Schröder
W. Fürst
A. Klein
R. Hurwitz
T. Zenk
J. Weber
K. Harzer
B. C. Paton
1 February 1992