DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.
about
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
@wuu
2017年学术文章
@zh
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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name
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@en
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@nl
type
label
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@en
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@nl
prefLabel
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@en
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@nl
P2093
P2860
P50
P356
P1433
P1476
DGUOK recessive mutations in p ...... kinsonism and mtDNA deletions.
@en
P2093
Chiara La Morgia
Elena Pegoraro
Francesca Tagliavini
Lidia Di Vito
Maria Lucia Valentino
Valerio Carelli
P2860
P356
10.1093/BRAIN/AWX301
P407
P577
2017-12-08T00:00:00Z