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CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are
CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are
CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are
CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are

CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are

SKU: 20396191870

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CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are

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Description

Defects in this gene are a cause of startle disease with epilepsy (STHEE)

it may play a key role in monitoring protein transport through the cell

Mutations in KRT17 lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex

This protein may interfere with the conversion of active

CT75 Rabbit Polyclonal Antibody, 20ul Isothermal Amplification Defects in this gene are

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