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RPR1B Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in this gene cause

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RPR1B Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in this gene cause

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Description

Mutations in this gene cause selective T-cell defect| a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells

indicating the implication of this gene in postmenopausal osteoporosis

This suggests it has a regulatory role in controlling cell shape and mobility

and thus acts as a regulator of angiogenesis

Expansion of a polyalanine tract and other mutations in this gene cause X-linked mental retardation and epilepsy

RPR1B Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in this gene cause

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