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

SKU: 2942695473

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

Store: aashay.com.au · Domain: aashay.com.au

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

ZDHHC20 (Zinc Finger DHHC-Type Containing 20) is a Protein Coding gene

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

The enzyme catalyzes the cleavage of big endothelin to produce the vasoconstrictor endothelin-1

This gene is located on a region of chromosome 17q21

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

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