OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
EMBO Molecular Medicine, EarlyView.
Source: EMBO Molecular Medicine - Category: Molecular Biology Authors: Kyle Thompson
,
Nicole Mai
,
Monika Ol áhová
,
Filippo Scialó
,
Luke E Formosa
,
David A Stroud
,
Madeleine Garrett
,
Nichola Z Lax
,
Fiona M Robertson
,
Cristina Jou
,
Andres Nascimento
,
Carlos Ortez
,
Cecilia Jimenez‐Malleb Source Type: research
More News: Molecular Biology