Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. (Q22008461)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. |
scientific article |
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Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. (English)
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Honsho M
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Tamura S
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Shimozawa N
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Suzuki Y
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Kondo N
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Fujiki Y
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