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VWA3A Polyclonal Antibody, 20ul Serum & Sample Tubes Mutations in this gene have

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VWA3A Polyclonal Antibody, 20ul Serum & Sample Tubes Mutations in this gene have

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Description

Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome

60S ribosomal protein L28 belongs to the L28E family of ribosomal proteins

Alternatively spliced transcript variants encoding different isoforms have been characterized

Diseases associated with CEBPB includeShort-Rib Thoracic Dysplasia 1 With Or Without PolydactylyandShort-Rib Thoracic Dysplasia 2 With Or Without Polydactyly

characterized by hypertriglyceridemia

VWA3A Polyclonal Antibody, 20ul Serum & Sample Tubes Mutations in this gene have

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