Molecular genetic study of a Japanese family with Lesch-Nyhan syndrome: a point mutation at the consensus region of RNA splicing (HPRTKeio). [electronic resource]

By: Contributor(s): Producer: 19940621Description: 413-9 p. digitalISSN:
  • 0916-8478
Subject(s): Online resources: In: The Japanese journal of human genetics vol. 38
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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