Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation. [electronic resource]

By: Contributor(s): Producer: 20160602Description: E217-9 p. digitalISSN:
  • 1096-8652
Subject(s): Online resources: In: American journal of hematology vol. 90
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
No physical items for this record

Publication Type: Letter; Research Support, Non-U.S. Gov't

There are no comments on this title.

to post a comment.