Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B (Q24322938)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B |
scientific article |
Statements
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B (English)
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September 1998
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7
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1399-405
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9
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