The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy
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| Description | scientific article published on May 2004 |
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author: Tamara Potikha |
| Publication date | May 1, 2004 |
| Language | English |
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