Open AccessIdentification of PSMB5 as a genetic modifier of fragile X–associated tremor/ataxia syndrome
Author(s) -
Ha Eun Kong,
Jung Hwa Lim,
Alexander E. Linsalata,
Yunhee Kang,
Indranil Malik,
Emily G. Allen,
Yiqu Cao,
Lisa Shubeck,
Rich Johnston,
Yanting Huang,
Yanghong Gu,
Xiangxue Guo,
Michael E. Zwick,
Zhaohui Qin,
Thomas S. Wingo,
Jorge L. Juncos,
David L. Nelson,
Michael P. Epstein,
David J. Cutler,
Peter K. Todd,
Stephanie L. Sherman,
Stephen T. Warren,
Peng Jin
Publication year - 2022
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2118124119
Subject(s) - ataxia , neurodegeneration , penetrance , fmr1 , genetics , fragile x syndrome , intention tremor , trinucleotide repeat expansion , biology , fragile x , neuroscience , medicine , allele , phenotype , disease , gene