Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
about
Leber's hereditary optic neuropathy is multiorgan not mono-organA new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene.Mitochondrial disease: genetics and management.Progress in neuro-otology research in the last year.Recent advances in clinical neurogenetics.Pathophysiological mechanisms and functional hearing consequences of auditory neuropathy.Distributed abnormalities of brain white matter architecture in patients with dominant optic atrophy and OPA1 mutations.Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies.
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P2860
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
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2011年學術文章
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name
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@en
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@nl
type
label
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@en
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@nl
prefLabel
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@en
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@nl
P2093
P2860
P50
P1433
P1476
Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.
@en
P2093
Anthony Gravina
Fleur O'Hare
Johanna Tan
Lauren Henley
Lisa Rosenfeld
Lisa S Kearns
P2860
P2888
P304
P356
10.1007/S00415-011-6230-7
P577
2011-09-02T00:00:00Z