Description
For Zafra, I; Nebenfuehr, B; Golden, A (2021). Saul-Wilson Syndrome Missense Allele Does Not Show Obvious Golgi Defects in a C. elegans Model. microPublication Biology. 10.17912/micropub.biology.000373.
The authors correct the following:
Figure: Panel C above the image of the embryo, the Golgi marker strain genotype “ugtp-1p::GFP”
is corrected to: “GFP::ugtp-1”
Figure legend: Where Panel C is described, it states, “No co-localization of ER (SP12::GFP) and Golgi (ugtp-1::mChr) markers observed in 2-cell embryos.”
This is now corrected to: “No co-localization of ER (SP12::mChr) and Golgi (GFP::ugtp-1) markers observed in 2-cell embryos.”.
Reagents: The Golgi marker strain genotype is written as “WH351: pie-1::GFP::ugtp-1 + unc119(+)”
This is now corrected to: “WH351: pie-1p::GFP::ugtp-1 + unc119(+)”.