MOLECULAR DEFECTS OF THE GLYCINE 41 VARIANTS OF ALANINE:GLYOXYLATE AMINOTRANSFERASE ASSOCIATED WITH PRIMARY HYPEROXALURIA TYPE I
Autor: | Cellini, B., Montioli, R., Paiardini, Alessandro, Lorenzetto, A., Maset, F., Bellini, T., Oppici, E., Borri Voltattorni, C. |
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Rok vydání: | 2010 |
Databáze: | OpenAIRE |
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