Published in
Oxford University Press (OUP), Brain, 1(141), p. e3-e3
DOI: 10.1093/brain/awx301
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DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions
Journal article published in 2017 by
Leonardo Caporali 
,
Luca Bello ,
Francesca Tagliavini,
Chiara La Morgia,
Alessandra Maresca ,
Lidia Di Vito,
Rocco Liguori,
Maria Lucia Valentino,
Diego Cecchin,
Elena Pegoraro,
Valerio Carelli
,
Luca Bello ,
Francesca Tagliavini,
Chiara La Morgia,
Alessandra Maresca ,
Lidia Di Vito,
Rocco Liguori,
Maria Lucia Valentino,
Diego Cecchin,
Elena Pegoraro,
Valerio Carelli
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
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