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Rui Feng

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Open access Sep 2026

Clinical characteristics of newborns with the deafness-associated GJB2 variant p.V37I in Changzhi, China

It is demonstrated that GJB2 variant p.V37I is significantly associated with neonatal hearing loss, underscoring its importance for inclusion in genetic screening programs to facilitate early intervention.

Rui Feng, E. Mangantig, Wan Shahriman Yushdie Wan Yusoff et al. · 0 citations

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