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1
Q

Transcription

A

Thalassemias and hereditary persistence of fetal hemoglobin

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2
Q

Translation

A

Thalassemias

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3
Q

Polypeptide folding

A

hemoglobinopathies

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4
Q

post-translational modification

A

I-cell disease (failure to add a phosphate group)

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5
Q

assembly of monomers into a holomeric protein

A

osteogenesis imperfecta

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6
Q

subcellular localization of the polypeptide of the holomer

A

familial hypercholesterolemia

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7
Q

cofactor or prosthetic group binding to the polypeptide

A

homocystinuria

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8
Q

function of a correctly folded, assembled and localized protein produced in normal amounts

A

Hb Kempsey

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