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Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological study. [electronic resource] by
- Schlote, W
- Harzer, K
- Christomanou, H
- Paton, B C
- Kustermann-Kuhn, B
- Schmid, B
- Seeger, J
- Beudt, U
- Schuster, I
- Langenbeck, U
Producer: 19911230
In:
European journal of pediatrics vol. 150
Availability: No items available.
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