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Page 1
Primary oxidative phosphorylation defects lead to perturbations in the human B cell repertoire.
Gordon-Lipkin EM, Banerjee P, Franco JLM, Tarasenko T, Kruk S, Thompson E, Gildea DE, Zhang S, Wolfsberg TG; NISC Comparative Sequencing Program; Flegel WA, McGuire PJ. Gordon-Lipkin EM, et al. Among authors: kruk s. Front Immunol. 2023 Jul 7;14:1142634. doi: 10.3389/fimmu.2023.1142634. eCollection 2023. Front Immunol. 2023. PMID: 37483601 Free PMC article.
Undiagnosed COVID-19 in households with a child with mitochondrial disease.
Gordon-Lipkin EM, Marcum C, Kruk S, Thompson E, Kelly SEM, Kalish H, Sadtler K, McGuire PJ. Gordon-Lipkin EM, et al. Among authors: kruk s. medRxiv [Preprint]. 2022 Mar 23:2022.03.21.22272358. doi: 10.1101/2022.03.21.22272358. medRxiv. 2022. PMID: 35350208 Free PMC article. Updated. Preprint.
Progressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum.
Sturrock BRH, Macnamara EF, McGuire P, Kruk S, Yang I, Murphy J; Undiagnosed Diseases Network; Tifft CJ, Gordon-Lipkin E. Sturrock BRH, et al. Among authors: kruk s. Mol Genet Genomic Med. 2021 Jun;9(6):e1692. doi: 10.1002/mgg3.1692. Epub 2021 May 7. Mol Genet Genomic Med. 2021. PMID: 33960148 Free PMC article.