Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease. [electronic resource]
Producer: 19981203Description: 1427-32 p. digitalISSN:- 0028-3878
- Bile Acids and Salts -- blood
- Cells, Cultured
- Diagnosis, Differential
- Erythrocytes -- metabolism
- Fatal Outcome
- Fatty Acids, Nonesterified -- blood
- Female
- Fibroblasts -- metabolism
- Humans
- Infant
- Intelligence
- Liver -- metabolism
- Microbodies -- metabolism
- Muscle, Skeletal -- pathology
- Pipecolic Acids -- blood
- Spinal Muscular Atrophies of Childhood -- diagnosis
- Zellweger Syndrome -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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