Pandolfo, M., Rai, M., Remiche, G., Desmyter, L., & Vandernoot, I. (2020). Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation. Neurol Genet.
Styl ChicagoPandolfo, Massimo, Myriam Rai, Gauthier Remiche, Laurence Desmyter, a Isabelle Vandernoot. "Cerebellar Ataxia, Neuropathy, Hearing Loss, and Intellectual Disability Due to AIFM1 Mutation." Neurol Genet 2020.
Citace podle MLAPandolfo, Massimo, et al. "Cerebellar Ataxia, Neuropathy, Hearing Loss, and Intellectual Disability Due to AIFM1 Mutation." Neurol Genet 2020.
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