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Novel ERCC2 mutation in two siblings with trichothiodystrophy.
Lund EB, Stein SL. Novel ERCC2 mutation in two siblings with trichothiodystrophy. Pediatr Dermatol. 2019 Sep; 36(5):668-671.
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PubMed
subject areas
Female
Humans
Infant
Infant, Newborn
Male
Mutation
Siblings
Trichothiodystrophy Syndromes
Xeroderma Pigmentosum Group D Protein
authors with profiles
Sarah Stein
Emily Lund
Novel ERCC2 mutation in two siblings with trichothiodystrophy.