Seppala, R., Lehto, V. P., & Gahl, W. A. (1999). Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzyme.
Čikaški stil citiranjaSeppala, R., V P. Lehto, i W A. Gahl. Mutations in the Human UDP-N-acetylglucosamine 2-epimerase Gene Define the Disease Sialuria and the Allosteric Site of the Enzyme. 1999.
MLA način citiranjaSeppala, R., V P. Lehto, i W A. Gahl. Mutations in the Human UDP-N-acetylglucosamine 2-epimerase Gene Define the Disease Sialuria and the Allosteric Site of the Enzyme. 1999.
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