APA引用形式

Smets, K., Duarri, A., Deconinck, T., Ceulemans, B., van de Warrenburg, B. P., Züchner, S., . . . Baets, J. (2015). First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy. BMC Med Genet.

シカゴスタイル引用形

Smets, Katrien, et al. "First De Novo KCND3 Mutation Causes Severe Kv4.3 Channel Dysfunction Leading to Early Onset Cerebellar Ataxia, Intellectual Disability, Oral Apraxia and Epilepsy." BMC Med Genet 2015.

MLA引用形式

Smets, Katrien, et al. "First De Novo KCND3 Mutation Causes Severe Kv4.3 Channel Dysfunction Leading to Early Onset Cerebellar Ataxia, Intellectual Disability, Oral Apraxia and Epilepsy." BMC Med Genet 2015.