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Función del gen Whsc1 durante el desarrollo embrionario de ratón

2019
Wolf-Hirschhorn syndrome (WHS) is a rare disease caused by hemizygous subtelomeric deletions of the distal region of the short arm of chromosome 4 (region 4p16.3). Of the different genes that are lost with this deletion, it is the Whsc1 gene, which codes for a histone methyltransferase, the main candidate to be responsible for the different symptoms ...
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