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 (Q40555085)
Jump to navigation
Jump to search
scientific article published on May 2004
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article published on May 2004 |
Statements
1 reference
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 (English)
1 reference
Stephan Hinderlich
1 reference
Ilan Salama
1 reference
Iris Eisenberg
1 reference
Tamara Potikha
1 reference
Lars R Mantey
1 reference
Kevin J Yarema
1 reference
Rüdiger Horstkorte
1 reference
Zohar Argov
1 reference
Menachem Sadeh
1 reference
Werner Reutter
1 reference
Stella Mitrani-Rosenbaum
1 reference
1 May 2004
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference