Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
about
Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob diseaseDifferential Expression of Complement Markers in Normal and AMD Transmitochondrial CybridsOphthalmic genetics: moving forward.Profound vision loss impairs psychological well-being in young and middle-aged individuals.Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.
P2860
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
description
2011 nî lūn-bûn
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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@ast
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@en
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@nl
type
label
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@ast
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@en
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@nl
prefLabel
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@ast
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@en
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@nl
P2860
P356
P1476
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
@en
P2093
Khaled K Abu-Amero
P2860
P356
10.4103/0974-9233.75880
P407
P577
2011-01-01T00:00:00Z