Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ‐line de novo mutation

Publisher: John Wiley & Sons Inc

E-ISSN: 1096-8652|90|12|E217-E219

ISSN: 0361-8609

Source: AMERICAN JOURNAL OF HEMATOLOGY, Vol.90, Iss.12, 2015-12, pp. : E217-E219

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Abstract