Identification of a stop mutation in five Finnish patients suffering from hereditary tyrosinemia type I. [electronic resource]

By: Contributor(s): Producer: 19940523Description: 69-72 p. digitalISSN:
  • 0964-6906
Subject(s): Online resources: In: Human molecular genetics vol. 3
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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