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Novel ERCC2 mutation in two siblings with trichothiodystrophy.
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has major subject area list
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Mutation; Siblings; Trichothiodystrophy Syndromes; Xeroderma Pigmentosum Group D Protein
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information resource reference
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Lund EB, Stein SL. Novel ERCC2 mutation in two siblings with trichothiodystrophy. Pediatr Dermatol. 2019 Sep; 36(5):668-671.
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label
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Novel ERCC2 mutation in two siblings with trichothiodystrophy.
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