OXA 1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
Journal article published in 2018 by
Kyle Thompson,
Nicole Mai,
Monika Oláhová,
Filippo Scialó,
Luke E. Formosa,
David A. Stroud,
Madeleine Garrett,
Nichola Z. Lax,
Fiona M. Robertson,
Cristina Jou,
Andres Nascimento,
Carlos Ortez 
,
Cecilia Jimenez‐Mallebrera,
Steven A. Hardy,
Langping He
and other authors.
,
Cecilia Jimenez‐Mallebrera,
Steven A. Hardy,
Langping He
and other authors.
This paper is made freely available by the publisher.
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