Open AccessDGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions
Author(s) -
Leonardo Caporali,
Luca Bello,
Francesca Tagliavini,
Chiara La Morgia,
Alessandra Maresca,
Lidia Di Vito,
Rocco Liguori,
Maria Lucia Valentino,
Diego Cecchin,
Elena Pegoraro,
Valério Carelli
Publication year - 2017
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awx301
Subject(s) - mitochondrial myopathy , mitochondrial dna , parkinsonism , genetics , biology , chronic progressive external ophthalmoplegia , mutation , mitochondrial disease , external ophthalmoplegia , medicine , gene , pathology , disease
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