TLS Online TPP Program

#Question id: 32222


Mutations in any of a dozen different peroxins, the most common being Pex1, cause an impairment in peroxisomal protein import, leads to:

#Unit 2. Cellular Organization
  1. Inclusion-cell disease
  2. Hurler’s disease
  3. Familial hypercholesterolemia
  4. Zellweger syndrome