Huntingtin Associates with Acidic Phospholipids at the Plasma Membrane
Kimberly B. Kegel(Harvard University), Marian DiFiglia(Massachusetts General Hospital), Lindsay Sobin(Massachusetts General Hospital), Neil Aronin(University of Massachusetts Chan Medical School), Zheng‐Hong Qin(Zunyi Medical University), Michael R. Hayden(University of British Columbia), Wolfgang H. Goldmann(Friedrich-Alexander-Universität Erlangen-Nürnberg), Ellen Sapp(Massachusetts General Hospital), Benjamin Cuiffo(Beth Israel Deaconess Medical Center), Yun Joong Kim(Yonsei University), G. Isenberg(Technical University of Munich), David L. Scott(Oregon Health & Science University), Jennifer Yoder(Massachusetts General Hospital)
Cited by 169
Related Papers
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
|Nature Genetics|1999|1.7k
Huntington disease
|Nature Reviews Disease Primers|2015|1.6k
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
|Nature Genetics|2003|976