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C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized
C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized
C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized
C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized

C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized

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C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized

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Description

a common congenital disorder characterized by neural-crest-related developmental defects

Mutations in this gene may play a role in familial idiopathic basal ganglia calcification

The protein is expressed in the photoreceptor layer of the retina| and the gene is mutated in autosomal recessive retinitis pigmentosa

FRS3 encodes a substrate for the fibroblast growth factor receptor

C16L2 Polyclonal Antibody, 20ul Vessels a common congenital disorder characterized

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