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SGPL1 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging Mutations in this gene are

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SGPL1 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging Mutations in this gene are

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Description

Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities

chloroquine

Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency

another member of the integrin family

This gene encodes a member of a family of serine/threonine protein kinases that participate in cell cycle regulation

SGPL1 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging Mutations in this gene are

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