Homo sapiens potassium inwardly rectifying channel subfamily J member - Nucleotide

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Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia. [Mov Disord. 2024]
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia.
Wirth T, Roze E, Delvallée C, Trouillard O, Drouot N, Damier P, Boulay C, Bourgninaud M, Jegatheesan P, Sangare A, et al. Mov Disord. 2024 May; 39(5):897-905. Epub 2024 Mar 4.
[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.

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Homo sapiens cyclin B1 interacting protein 1 (CCNB1IP1), transcript variant 2, m...
Homo sapiens cyclin B1 interacting protein 1 (CCNB1IP1), transcript variant 2, mRNA
gi|1890263857|ref|NM_182849.3|

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Nucleotide