TY  - GEN
AU  - Moser,H W
TI  - Peroxisomal diseases
SN  - 0065-3101
PY  - 1989///1019
KW  - Congenital Abnormalities
KW  - diagnosis
KW  - Humans
KW  - Infant, Newborn
KW  - Microbodies
KW  - enzymology
N1  - Publication Type: Journal Article; Review
ER  -