atypical Gaucher's disease due to saposin c deficiency (Q32145296)
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A Gaucher's disease that has material basis in an autosomal recessive mutation of PSAP on chromosome 10q22.1.
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | atypical Gaucher's disease due to saposin c deficiency |
A Gaucher's disease that has material basis in an autosomal recessive mutation of PSAP on chromosome 10q22.1. |
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