TY  - GEN
AU  - Baumgartner,M R
AU  - Verhoeven,N M
AU  - Jakobs,C
AU  - Roels,F
AU  - Espeel,M
AU  - Martinez,M
AU  - Rabier,D
AU  - Wanders,R J
AU  - Saudubray,J M
TI  - Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease
SN  - 0028-3878
PY  - 1998///1203
KW  - Bile Acids and Salts
KW  - blood
KW  - Cells, Cultured
KW  - Diagnosis, Differential
KW  - Erythrocytes
KW  - metabolism
KW  - Fatal Outcome
KW  - Fatty Acids, Nonesterified
KW  - Female
KW  - Fibroblasts
KW  - Humans
KW  - Infant
KW  - Intelligence
KW  - Liver
KW  - Microbodies
KW  - Muscle, Skeletal
KW  - pathology
KW  - Pipecolic Acids
KW  - Spinal Muscular Atrophies of Childhood
KW  - diagnosis
KW  - Zellweger Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/wnl.51.5.1427
ER  -