Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers. [electronic resource]

By: Contributor(s): Producer: 19940223Description: 531-6 p. digitalISSN:
  • 0006-4971
Subject(s): In: Blood vol. 83
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Publication Type: Case Reports; Journal Article

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