Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report.
González-Quintana A, García-Consuegra I, Belanger-Quintana A, Serrano-Lorenzo P, Lucia A, Blázquez A, Docampo J, Ugalde C, Morán M, Arenas J, Martín MA.
González-Quintana A, et al. Among authors: garcia consuegra i.
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Genes (Basel). 2020.
PMID: 32722639
Free PMC article.