Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
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A. Lehmann | J. Krutmann | S. Queillé | K. Kraemer | C. Arlett | A. Sarasin | M. Stefanini | T. Nardò | M. Berneburg | B. Broughton | E. Taylor | H. Fawcett | V. Price | E. Menefee | R. Davidson | E. Bohnert | Mark Berneburg | M. Berneburg