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In summary, we describe a mouse model of human deafness DFNB39 and demonstrate a functional link between a 10bp deletion in a highly conserved intronic sequence of Hgf and hereditary hearing loss

This conceptual approach might be further indicative of additional implementation of the cytoprotection concept into eye pharmacotherapy and the whole occlusion/occlusion-like syndrome [18,19,20,21,22,23,24,25,26,27,28,29,30]

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GHK-Cu modulates 127 genes related to inflammation, consistently upregulating repair genes while downregulating inflammatory markers

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