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Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria

✍ Scribed by Hava Peretz; Meirav Shtauber Naamati; David Levartovsky; Ayala Lagziel; Esther Shani; Ivona Horn; Hanna Shalev; Daniel Landau


Book ID
116987974
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
663 KB
Volume
91
Category
Article
ISSN
1096-7192

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