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. 2021 Mar 24;2021:10.17912/micropub.biology.000379. doi: 10.17912/micropub.biology.000379

Corrigendum: Saul-Wilson Syndrome Missense Allele Does Not Show Obvious Golgi Defects in a C. elegans Model

PMCID: PMC7991895  PMID: 33791595

Figure 1.

Figure 1.

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(+)”.


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