Homo sapiens potassium inwardly rectifying channel subfamily J member - Nucleotide

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[Analysis of genotypes on 850 newborns with SLC26A4 single-allele mutation and the phenotypes of those with second variant]. [Zhonghua Er Bi Yan Hou Tou Jin...]
[Analysis of genotypes on 850 newborns with SLC26A4 single-allele mutation and the phenotypes of those with second variant].
Huang LH, Zhao XL, Cheng XH, Yu YD, Wen C, Li Y, Wang XL, Wang XY, Ruan Y, En H. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2023 Feb 7; 58(2):117-125.
Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies. [Int J Mol Sci. 2022]
Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies.
Klarov LA, Pshennikova VG, Romanov GP, Cherdonova AM, Solovyev AV, Teryutin FM, Luginov NV, Kotlyarov PM, Barashkov NA. Int J Mol Sci. 2022 Dec 6; 23(23). Epub 2022 Dec 6.
Spinocerebellar ataxia in the Bouvier des Ardennes breed is caused by a KCNJ10 missense variant. [J Vet Intern Med. 2023]
Spinocerebellar ataxia in the Bouvier des Ardennes breed is caused by a KCNJ10 missense variant.
Stee K, Van Poucke M, Pumarola M, Geerinckx L, Van Soens I, Bhatti SFM, Peelman L, Cornelis I. J Vet Intern Med. 2023 Jan; 37(1):216-222. Epub 2022 Nov 25.

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Nucleotide