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  • Molecular assay reagents intended to identify mutations in the solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene, located at chromosome 5q31-q34, which encodes for a protein that transports ions, particularly sulfate ions, across cell membranes. This inherited genetic mutation has been identified in patients with diastrophic dysplasia (DTD) and atelosteogenesis type 2 (AO2, also known as neonatal osseous dysplasia type I).
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