Low, K., Stals, K., Caswell, R., Wakeling, M., Clayton-Smith, J., Donaldson, A., . . . Smithson, S. (2018). Phenotype of CNTNAP1: A study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy. Eur J Hum Genet.
Citación estilo ChicagoLow, KJ, et al. "Phenotype of CNTNAP1: A Study of Patients Demonstrating a Specific Severe Congenital Hypomyelinating Neuropathy With Survival Beyond Infancy." Eur J Hum Genet 2018.
Cita MLALow, KJ, et al. "Phenotype of CNTNAP1: A Study of Patients Demonstrating a Specific Severe Congenital Hypomyelinating Neuropathy With Survival Beyond Infancy." Eur J Hum Genet 2018.
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