Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema. [electronic resource]

By: Contributor(s): Producer: 20020830Description: 461 p. digitalISSN:
  • 1098-1004
Subject(s): Online resources: In: Human mutation vol. 19
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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