Analysis of slc26a4, foxi1, and kcnj10 gene variants in patients with incomplete partition of the cochlea and enlarged vestibular aqueduct (eva) anomalies

HIGHLIGHTS

• who: Leonid A. Klarov and colleagues from the SiberiaSiberiaYakut Science Centre of Complex Medical Problems, Yakutsk, Russia Laboratory of Molecular Biology, MKAmmosov North-Eastern Federal University, Yakutsk, Russia have published the paper: Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies, in the Journal: (JOURNAL) of 28/09/2022
• what: For the first time, the study demonstrated that in biallelic SLC26A4 patients all incomplete partitions of the cochlea are possible, from IP-1 and IP-2 to a normal cochlea.
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