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Q46401865-41B83183-7FAA-402B-9BE5-BCD900D3072D
Q46401865-41B83183-7FAA-402B-9BE5-BCD900D3072D
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http://www.wikidata.org/entity/statement/Q46401865-41B83183-7FAA-402B-9BE5-BCD900D3072D
Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1.
P2860
Q46401865-41B83183-7FAA-402B-9BE5-BCD900D3072D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46401865-41B83183-7FAA-402B-9BE5-BCD900D3072D
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wasDerivedFrom
03736c5447f1bf7324aab874fd5fdc320feb4b91
P2860
Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations