A review of the mechanisms underlying the role of the gipc3 gene in hereditary deafness

HIGHLIGHTS

• who: Xinxin Li and colleagues from the Hamamatsu University School of Medicine, Japan have published the paper: A review of the mechanisms underlying the role of the GIPC3 gene in hereditary deafness, in the Journal: (JOURNAL)

SUMMARY

Frontiers in Synaptic Neuroscience Deafness is a major global public health issue and a common human disorder. According to the World Hearing Report, which was released by the World Health Organization (WHO), more than 1.5 billion people have varying degrees of hearing loss worldwide (Chadha et_al, 2021; World Health Organization, 2021). As research has progressed . . .

 



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