Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature child.
about
Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutationsAnalysis of Genetic Mutations in a Cohort of Hereditary Optic Neuropathy in Shanghai, China.Idebenone in Friedreich ataxia and Leber's hereditary optic neuropathy: close mechanisms, similar therapy?
P2860
Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature child.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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name
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@en
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@nl
type
label
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@en
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@nl
prefLabel
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@en
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@nl
P2093
P2860
P356
P1476
Uncommon Leber "plus" disease ...... 11778G>A in a premature child.
@en
P2093
Anne Charon
Catherine Wetzburger
Dominique Roland
Françoise Meire
Isabelle Maystadt
Marie-Cécile Nassogne
Monique Cordonnier
Rudy Van Coster
Stéphanie Paquay
Valérie Benoit
P2860
P304
P356
10.1177/0883073813492895
P577
2013-07-17T00:00:00Z