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VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Defects in this gene are

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VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Defects in this gene areThis gene encodes a homeobox protein originally described as a retina specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.

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Description

Defects in this gene are a cause of Walker-Warburg syndrome (WWS)

Ku is the DNA-binding component of the DNA-dependent protein kinase

Members of the subfamily share similarity in sequence and splice sites

Deficiencies in this protein are associated with an increased risk of ischemic arterial diseases and fetal loss

This gene encodes the receptor for both luteinizing hormone and choriogonadotropin

VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Defects in this gene areThis gene encodes a homeobox protein originally described as a retina specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.

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