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MCT12 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos Defects in this gene are

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MCT12 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos Defects in this gene areSLC16A12 encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria.

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Description

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

The protein encoded by LAMA3 belongs to the laminin family of secreted molecules

and may play a role in lymphocyte homing to secondary lymphoid organs

and roles in inflammation and immune response

CAD (carbamoyl-phosphate synthetase 2

MCT12 Polyclonal Antibody, 20ul Diagnostic Probes & Oligos Defects in this gene areSLC16A12 encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria.

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