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

Saul-Wilson Syndrome is an ultra-rare skeletal syndrome caused by a mutation in the COG4 gene resulting in a glycine-to-arginine substitution at amino acid position 516. The COG4 gene encodes one of 8 subunits of the conserved oligomeric Golgi complex. Using CRISPR-Cas9, our lab generated a C. elega...

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Detalles Bibliográficos
Autores principales: Zafra, Isabella, Nebenfuehr, Benjamin, Golden, Andy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2021
Materias:
Negative Result
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933980/
https://www.ncbi.nlm.nih.gov/pubmed/33688625
http://dx.doi.org/10.17912/micropub.biology.000373

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933980/
https://www.ncbi.nlm.nih.gov/pubmed/33688625
http://dx.doi.org/10.17912/micropub.biology.000373

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