The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy (Q28214777)
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scientific article (publication date: September 2001)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy |
scientific article (publication date: September 2001) |
Statements
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy (English)
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September 2001
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29
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1
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83-7
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