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  • Molecular assay reagents intended to identify mutations in the sal-like 4 (SALL4) gene, located at chromosome 20q13.13-q13.2, which is part of a gene family that encodes for proteins involved in formation of tissue and organs in embryogenesis. This genetic mutation has been identified in patients with SALL4-related disorders, a spectrum of diseases that include Duane and anomaly radial-ray malformation (DARRM/Okihiro syndrome), acro-renal-ocular syndrome, and, less frequently, Holt-Oram syndrome.
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