Associated Papers
Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder.
Chiarelli LR et al.
Haematologica, 2006
Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations.
Zanella A et al.
British Journal of Haematology, 2006
Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutations.
Chiarelli LR et al.
Blood Cells, Molecules & Diseases, 0
Select a paper to view details