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One or more keywords matched the following properties of Novel ERCC2 mutation in two siblings with trichothiodystrophy.

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has major subject area list Mutation; Siblings; Trichothiodystrophy Syndromes; Xeroderma Pigmentosum Group D Protein
information resource reference Lund EB, Stein SL. 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.

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  • Siblings