González-Quintana, A., García-Consuegra, I., Belanger-Quintana, A., Serrano-Lorenzo, P., Lucia, A., Blázquez, A., . . . Martín, M. A. (2020). Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. Genes (Basel).
Styl ChicagoGonzález-Quintana, Adrián, et al. "Novel NDUFA13 Mutations Associated With OXPHOS Deficiency and Leigh Syndrome: A Second Family Report." Genes (Basel) 2020.
Citace podle MLAGonzález-Quintana, Adrián, et al. "Novel NDUFA13 Mutations Associated With OXPHOS Deficiency and Leigh Syndrome: A Second Family Report." Genes (Basel) 2020.
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