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Human Being Genetic Science Description Chromosomes Inheritance: Revision history

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30 October 2025

  • curprev 11:0711:07, 30 October 2025 LeathaLongoria6 talk contribs 9,485 bytes +9,485 Created page with "<br><br><br>ACH is caused by [https://www.martindale.com/Results.aspx?ft=2&frm=freesearch&lfd=Y&afs=taxonomic taxonomic] group variants in FGFR3, the cistron for fibroblast ontogeny agent (FGF) sense organ 3 (FGFR3), on chromosome 4p16. About wholly individuals with ACH are heterozygous for a chance variable which leads to a exchange of arginine for glycine at post 380 (p.Gly380Arg) in the maturate protein. Lxxx percentage of ACH cases are owed to spontaneous, de novo mu..."
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