Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
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MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis DisorderSevere inflammatory disease activity 14 months after cessation of Natalizumab in a patient with Leber's optic neuropathy and multiple sclerosis - a case reportOptimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON)Biomarkers for Detecting Mitochondrial Disorders.
P2860
Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
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2016 nî lūn-bûn
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2016 թվականի հունվարին հրատարակված գիտական հոդված
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2016年の論文
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2016年論文
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2016年論文
@zh-hant
2016年論文
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2016年論文
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2016年論文
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2016年论文
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2016年论文
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name
Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
@en
type
label
Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
@en
prefLabel
Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
@en
P2093
P2860
P1476
Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.
@en
P2093
Dean M Cestari
Nailyn Rasool
Simmons Lessell
P2860
P304
P356
10.3109/08820538.2015.1115251
P407
P577
2016-01-01T00:00:00Z