Concepedia

Publication | Open Access

<i> <scp>OXA</scp> 1L </i> mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

DOIFull Paper Access

84

Citations

43

References

2018

Year

Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialò, Luke E. Formosa, David A. Stroud, Madeleine Garrett, Nichola Z. Lax, Fiona Robertson, Cristina Jou,
EMBO Molecular Medicine

References

YearCitations

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