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    hypothetical protein Mrub_2349 [Meiothermus ruber DSM 1279]

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    • Peutz-Jeghers Syndrome
      Peutz-Jeghers Syndrome
      A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and...<br/>Year introduced: 1965
      MeSH

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