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NTAL Polyclonal Antibody, 50ul Cell Culture Dishes autosomal dominant iridogoniodysgenesis anomaly

SKU: 32277896594

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NTAL Polyclonal Antibody, 50ul Cell Culture Dishes autosomal dominant iridogoniodysgenesis anomalyThis gene is one of the contiguous genes at 7q11. 23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.

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Description

autosomal dominant iridogoniodysgenesis anomaly

and binding viral RNAs associated with hepatitis C virus

is expressed in a variety of tissues with the highest levels in heart and pancreas

MIM 603492) and interacts with the adaptor molecule SAP (SH2D1A

a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions

NTAL Polyclonal Antibody, 50ul Cell Culture Dishes autosomal dominant iridogoniodysgenesis anomalyThis gene is one of the contiguous genes at 7q11. 23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.

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