Williams-Beuren Syndrome Related Methyltransferase WBSCR27: From Structure to Possible Function
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DOI: 10.3389/fmolb.2022.865743
Abstract: Williams-Beuren syndrome (WBS) is a genetic disorder associated with the hemizygous deletion of several genes in chromosome 7, encoding 26 proteins. Malfunction of these proteins induce multisystemic failure in an organism. While biological functions of… read more here.
Keywords: methyltransferase wbscr27; williams beuren; structure; beuren syndrome ... See more keywords