Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Novel ERCC2 mutation in two siblings with trichothiodystrophy.
See All Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Novel ERCC2 mutation in two siblings with trichothiodystrophy.
Novel ERCC2 mutation in two siblings with trichothiodystrophy. Pediatr Dermatol. 2019 Sep; 36(5):668-671.
View in:
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