Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a complex, late-onset, neurodegenerative disease with a genetic contribution to disease liability. Genome-wide association studies (GWAS) have identified ten risk loci to date, including the TNIP1/GPX3 locus on chromosome five. Given association ana...

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Detalles Bibliográficos
Autores principales: Restuadi, Restuadi, Steyn, Frederik J., Kabashi, Edor, Ngo, Shyuan T., Cheng, Fei-Fei, Nabais, Marta F., Thompson, Mike J., Qi, Ting, Wu, Yang, Henders, Anjali K., Wallace, Leanne, Bye, Chris R., Turner, Bradley J., Ziser, Laura, Mathers, Susan, McCombe, Pamela A., Needham, Merrilee, Schultz, David, Kiernan, Matthew C., van Rheenen, Wouter, van den Berg, Leonard H., Veldink, Jan H., Ophoff, Roel, Gusev, Alexander, Zaitlen, Noah, McRae, Allan F., Henderson, Robert D., Wray, Naomi R., Giacomotto, Jean, Garton, Fleur C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767698/
https://www.ncbi.nlm.nih.gov/pubmed/35042540
http://dx.doi.org/10.1186/s13073-021-01006-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767698/
https://www.ncbi.nlm.nih.gov/pubmed/35042540
http://dx.doi.org/10.1186/s13073-021-01006-6

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