<?xml version="1.0" encoding="UTF-8"?>
<references>
<reference>
  <a1>Pacheu-Grau, David</a1>
  <a2>Callegari, Sylvie</a2>
  <a2>Emperador, Sonia</a2>
  <a2>Thompson, Kyle</a2>
  <a2>Aich, Abhishek</a2>
  <a2>Topol, Sarah E.</a2>
  <a2>Spencer, Emily G.</a2>
  <a2>McFarland, Robert</a2>
  <a2>Ruiz-Pesini, Eduardo</a2>
  <a2>Torkamani, Ali</a2>
  <a2>Taylor, Robert W.</a2>
  <a2>Montoya, Julo</a2>
  <a2>Rehling, Peter</a2>
  <t1>Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy</t1>
  <t2>Hum. mol. genet.</t2>
  <sn/>
  <op/>
  <vo/>
  <ab/>
  <la>eng</la>
  <k1/>
  <pb/>
  <pp/>
  <yr>2018</yr>
  <ed/>
  <ul>http://zaguan.unizar.es/record/79519/files/texto_completo.pdf;
	http://zaguan.unizar.es/record/79519/files/texto_completo.jpg?subformat=icon;
	</ul>
  <no>Imported from Invenio.</no>
</reference>

</references>