The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Iris Eisenberg, Nili Avidan, Tamara Potikha, Hagit Hochner, Miriam Chen, Tsviya Olender, Mark Barash, Moshe Shemesh, Menachem Sadeh, Gil Grabov-Nardini, Inna Shmilevich, Adam Friedmann, George Karpati, Walter G. Bradley, Lisa Baumbach, Doron Lancet, Edna Ben Asher, Jacques S. Beckmann, Zohar Argov, Stella Mitrani-Rosenbaum*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

473 Scopus citations

Fingerprint

Dive into the research topics of 'The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology

Neuroscience

Keyphrases