Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease. [electronic resource]

By: Contributor(s): Producer: 19980601Description: 832-6 p. digitalISSN:
  • 0022-202X
Subject(s): Online resources: In: The Journal of investigative dermatology vol. 110
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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