Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease highlight shared and tissue-specific effects
Group 1, Jong‐Min Lee, Zachariah L. McLean, Kevin Correia, Jun Wan Shin, Sujin Lee, Jae-Hyun Jang, Yukyeong Lee, Kyung‐Hee Kim, Doo Eun Choi, Jeffrey D. Long, Diane Lucente, Ihn Sik Seong, Ricardo Mouro Pinto, James V. Giordano, Jayalakshmi Srinidhi Mysore, Jacqueline Siciliano, Emanuela Elezi, Jayla Ruliera, Tammy Gillis, Vanessa C. Wheeler, Marcy E. MacDonald, James F. Gusella, Group 2, Anna Gatseva, Marc Ciosi, Vilija Lomeikaite, Hossameldin Loay, Darren G. Monckton, Group 3, Christopher Wills, Thomas H. Massey, Lesley Jones, Peter Holmans, Group 4, Seung Kwak, Cristina Sampaio, Group 5, Michael Orth, G. Bernhard Landwehrmeyer, Jane S. Paulsen, E. Ray Dorsey, Richard H. Myers
Topics & Concepts
BiologyPMS2Somatic cellTrinucleotide repeat expansionGeneticsPhenotypeHuntington's diseaseGeneDNA repairDiseaseDNA mismatch repairAllelePathologyMedicineGenetic Neurodegenerative DiseasesMitochondrial Function and PathologyMuscle Physiology and Disorders