Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

2013/03/01 by Hong Joo Kim, Nam Chul Kim, Yong-Dong Wang +44 · 3 citations
Biochemistry, Genetics and Molecular Biology · Medicine · #Amyotrophic Lateral Sclerosis Research #Prion Diseases and Protein Misfolding #RNA Research and Splicing

paper · doi:10.1038/nature11922

crossref issued 2013/03/01 · crossref published 2013/03/01 · crossref published-print 2013/03/01 · openalex publication_date 2013/03/01 · crossref created 2013/03/01 · crossref published-online 2013/03/03 · crossref deposited 2023/05/18 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/01 · crossref indexed 2026/08/05

Citations

• Sarcoplasmic redistribution of nuclear TDP‐43 in inclusion body myositis

Cited by

• Self-propagation of pathogenic protein aggregates in neurodegenerative diseases
• Long-term memory consolidation: The role of RNA-binding proteins with prion-like domains
• Prion [wikipedia]