Homo sapiens KIAA1985 (KIAA1985) mRNA, complete cds

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Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian Cohort. [Neurol India. 2023]
Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian Cohort.
Nagappa M, Sharma S, Govindaraj P, Chickabasaviah YT, Siram R, Shroti A, Seshagiri DV, Debnath M, Sinha S, Bindu PS, et al. Neurol India. 2023 Sep-Oct; 71(5):940-945.
Evaluation of Pathogenicity and Causativity of Variants in the MPZ and SH3TC2 Genes in a Family Case of Hereditary Peripheral Neuropathy. [Int J Mol Sci. 2023]
Evaluation of Pathogenicity and Causativity of Variants in the MPZ and SH3TC2 Genes in a Family Case of Hereditary Peripheral Neuropathy.
Shchagina O, Orlova M, Murtazina A, Filatova A, Skoblov M, Dadali E. Int J Mol Sci. 2023 Jun 6; 24(12). Epub 2023 Jun 6.
Screening for SH3TC2 variants in Charcot-Marie-Tooth disease in a cohort of Chinese patients. [Acta Neurol Belg. 2022]
Screening for SH3TC2 variants in Charcot-Marie-Tooth disease in a cohort of Chinese patients.
Sun B, He ZQ, Li YR, Bai JM, Wang HR, Wang HF, Cui F, Yang F, Huang XS. Acta Neurol Belg. 2022 Oct; 122(5):1169-1175. Epub 2021 Feb 15.

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Nucleotide