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Biochemical characterization of the M712T-mutation of the UDP-N-acetylglucosamine 2-epimerase/N-acetyl-mannosaminekinase in hereditary inclusion body myopathy

✍ Scribed by Wenke Weidemann; Anika Reinhardt; Annett Thate; Rüdiger Horstkorte

Book ID: 116794807
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 682 KB
Volume: 21
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2011.06.004

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