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Items: 6

1.
2.

PGK deficiency.

Beutler E.

Br J Haematol. 2007 Jan;136(1):3-11. Review.

PMID:
17222195
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4.

Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.

Miwa S, Fujii H.

Am J Hematol. 1985 Jul;19(3):293-305. Review.

PMID:
2990202
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6.

A novel missense mutation (1060G --> C) in the phosphoglycerate kinase gene in a Japanese boy with chronic haemolytic anaemia, developmental delay and rhabdomyolysis.

Morimoto A, Ueda I, Hirashima Y, Sawai Y, Usuku T, Kano G, Kuriyama K, Todo S, Sugimoto T, Kanno H, Fujii H, Imashuku S.

Br J Haematol. 2003 Sep;122(6):1009-13. Review.

PMID:
12956773

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