논문KCI 등재
A Novel KCND3 Variant in a Korean Family With SCA19
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참고문헌 (7)
- Klockgether T, "Spinocerebellar ataxia", Nat Rev Dis Primers, 5, pp.24~ (2019)
- 김민경, "Extracerebellar Signs and Symptoms in 117 Korean Patients with Early-Stage Spinocerebellar Ataxia", Journal of Clinical Neurology, 17(2), pp.242~248 (2021), 대한신경과학회
- Serôdio P, "Cloning of a novel compo"nent of A-type K+ channels operating at subthreshold potentials with unique expression in heart and brain", J Neurophysiol, 75, pp.2174~2179 (1996)
- Pollini L, "KCND3-related neurological disorders : from old to emerging clini"cal phenotypes", Int J Mol Sci, 21, pp.5802~ (2020)
- Seidel K, "First patho-anatomical investigation of the brain of a SCA19patient", Neuropathol Appl Neurobiol, 40, pp.640~644 (2014)
- Duarri A, "Mutations in potassium channel kcnd3 cause spinocer"ebellar ataxia type 19", Ann Neurol, 72, pp.870~880 (2012)
- Lee YC, "Mutations in KCND3 cause spinocerebellar ataxia type 22", Ann Neu"rol, 72, pp.859~886 (2012)
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