Biochemical phenotype of a common disease-causing mutation...

Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylation

Andreotti, Giuseppina, Pedone, Emilia, Giordano, Assunta, Cubellis, Maria Vittoria
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Volume:
1
Language:
english
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.3
Date:
May, 2013
File:
PDF, 745 KB
english, 2013
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