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Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder
Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder
Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder
Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder

Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder

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Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder

Store: cgm.lt · Domain: cgm.lt

Description

an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome

This gene is expressed in germinal center B-cells

juvenile polyposis syndrome

via endocytosis of hemoglobin/haptoglobin and subsequent breakdown of heme

Multiple transcript variants encoding different isoforms have been found for PTGER3

Human Golgin Subfamily B Member 1, GOLGB1 ELISA Kit, 96T Culture Plate Inserts an autosomal recessive neurologic disorder

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