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No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation

✍ Scribed by Ilan Salama; Stephan Hinderlich; Zipora Shlomai; Iris Eisenberg; Sabine Krause; Kevin Yarema; Zohar Argov; Hanns Lochmuller; Werner Reutter; Ron Dabby; Menachem Sadeh; Hannah Ben-Bassat; Stella Mitrani-Rosenbaum


Book ID
116289843
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
366 KB
Volume
328
Category
Article
ISSN
0006-291X

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