APA Alıntı

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.

Chicago Stili Alıntı

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 Alıntı

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.