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Novel ERCC2 mutation in two siblings with trichothiodystrophy.
One or more keywords matched the following properties of Novel ERCC2 mutation in two siblings with trichothiodystrophy.
PropertyValue
has major subject area list Mutation; Siblings; Trichothiodystrophy Syndromes; Xeroderma Pigmentosum Group D Protein
information resource reference Novel ERCC2 mutation in two siblings with trichothiodystrophy. Pediatr Dermatol. 2019 Sep; 36(5):668-671.
label Novel ERCC2 mutation in two siblings with trichothiodystrophy.
Search Criteria
  • Siblings