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Changes in Biophysical Characteristics of PFN1 Due to Mutation Causing Amyotrophic Lateral Sclerosis

Single amino acid mutations in profilin 1 (PFN1) have been found to cause amyotrophic lateral sclerosis (ALS). Recently, we developed a mouse model for ALS using a PFN1 mutation (glycine 118 to valine, G118V), and we are now interested in understanding how PFN1 becomes toxically lethal with only one...

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Detaylı Bibliyografya
Yayımlandı:Metab Brain Dis
Asıl Yazarlar: Nekouei, Mina, Ghezellou, Parviz, Aliahmadi, Atousa, Arjmand, Sareh, Kiaei, Mahmoud, Ghassempour, Alireza
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6230493/
https://ncbi.nlm.nih.gov/pubmed/30203378
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11011-018-0305-4
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