Transcription
Thalassemias and hereditary persistence of fetal hemoglobin
Translation
Thalassemias
Polypeptide folding
hemoglobinopathies
post-translational modification
I-cell disease (failure to add a phosphate group)
assembly of monomers into a holomeric protein
osteogenesis imperfecta
subcellular localization of the polypeptide of the holomer
familial hypercholesterolemia
cofactor or prosthetic group binding to the polypeptide
homocystinuria
function of a correctly folded, assembled and localized protein produced in normal amounts
Hb Kempsey