Gene Mutations: Revision history

From Rest of What I Know

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8 January 2025

15 November 2024

  • curprev 23:4423:44, 15 November 2024‎ Roshan talk contribs‎ 6,743 bytes +6,743‎ Created page with "Both Julie and I are carriers of a gene mutation in the GJB-2 gene. This makes it quite likely that our children will have what is called non-syndromic hearing loss, i.e. they will be born deaf or hard of hearing without other changes to the body. == GJB-2 Gene Problems == The Gap Junction<ref name="gap-junction" />Protein Beta-2 (GJB-2) gene codes for<ref name="dna-basics"/> the protein Connexin-26. As you can imagine, a protein can break in many ways. One common way..."
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