A LYSOSOMAL STORAGE DISORDER IN MICE CHARACTERIZED BY A DUAL DEFICIENCY OF SPHINGOMYELINASE AND GLUCOCEREBROSIDASE

[1] BOOTHE AD, 1977, FED PROC, V36, P1158

[2] Brady R.O., 1978, METABOLIC BASIS INHE, P718

[3] REPLACEMENT THERAPY FOR INHERITED ENZYME DEFICIENCY - USE OF PURIFIED GLUCOCEREBROSIDASE IN GAUCHERS-DISEASE [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1974, 291 (19) : 989 - 993

[4] BRUNNGRABER EG, 1976, ADV EXPT MEDICINE BI, V68, P33

[5] NEUROCHEMISTRY OF MUCOPOLYSACCHARIDOSES - BRAIN GLYCOSAMINOGLYCANS IN NORMALS AND 4 TYPES OF MUCOPOLYSACCHARIDOSES [J]. JOURNAL OF NEUROCHEMISTRY, 1976, 26 (05) : 901 - &

[6] DAWSON G, 1972, J LIPID RES, V13, P207

[7] Dittmer J, 1969, METHOD ENZYMOL, V14, P482, DOI [10.1016/S0076-6879(69)14055-0, DOI 10.1016/S0076-6879(69)14055-0]

[8] FISHMAN PH, 1979, DENSITOMETRY THIN LA, P315

[9] KWITEROVICH PO, 1970, J LIPID RES, V11, P322

[10] MORRIS MD, 1977, FED PROC, V36, P1158

[1] BOOTHE AD, 1977, FED PROC, V36, P1158

[2] Brady R.O., 1978, METABOLIC BASIS INHE, P718

[3] REPLACEMENT THERAPY FOR INHERITED ENZYME DEFICIENCY - USE OF PURIFIED GLUCOCEREBROSIDASE IN GAUCHERS-DISEASE [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1974, 291 (19) : 989 - 993

[4] BRUNNGRABER EG, 1976, ADV EXPT MEDICINE BI, V68, P33

[5] NEUROCHEMISTRY OF MUCOPOLYSACCHARIDOSES - BRAIN GLYCOSAMINOGLYCANS IN NORMALS AND 4 TYPES OF MUCOPOLYSACCHARIDOSES [J]. JOURNAL OF NEUROCHEMISTRY, 1976, 26 (05) : 901 - &

[6] DAWSON G, 1972, J LIPID RES, V13, P207

[7] Dittmer J, 1969, METHOD ENZYMOL, V14, P482, DOI [10.1016/S0076-6879(69)14055-0, DOI 10.1016/S0076-6879(69)14055-0]

[8] FISHMAN PH, 1979, DENSITOMETRY THIN LA, P315

[9] KWITEROVICH PO, 1970, J LIPID RES, V11, P322

[10] MORRIS MD, 1977, FED PROC, V36, P1158