Purpose
Expresses NSDHL harboring all currently known mutations within exons 4 and 6 associated with CHILD syndrome.
Insert
human NSDHL with mutations in exon 4 and exon 6 (
NSDHL Human, Synthetic)
Mutation
C>T = A105V; G>C = A182P; G>A = R199H; G…
Available Since
March 5, 2020
Availability
Academic Institutions and Nonprofits only