The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy (Q28214777)
(Redirected from Q28183241)
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)
0 references
September 2001
0 references
29
0 references
83-7
0 references
1
0 references