Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndrome.

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Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndrome.

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Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

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Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

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Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

@en

Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

@nl

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Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

@en

Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

@nl

P1476

Complete mtDNA sequencing reve ...... patients with Leigh syndrome.

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Algirdas Utkus

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Baiba Lace

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Birute Burnyte

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Eriks Jankevics

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Evelina Dagyte

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Irina Adomaitiene

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Janis Stavusis

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Jolanta Rozentale

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Kristina Grigalioniene

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Liana Pliss

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P2860

Subacute necrotizing encephalomyelopathy in an infant

HMDB 3.0--The Human Metabolome Database in 2013

Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.

Do the four clades of the mtDNA haplogroup L2 evolve at different rates?

Two new mutations in the MTATP6 gene associated with Leigh syndrome.

A mitochondrial bioenergetic etiology of disease.

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

Leigh and Leigh-like syndrome in children and adults.

Central retinal vein occlusion as the initial manifestation of LHON / MELAS overlap syndrome with mitochondrial DNA G13513A mutation--case report and literature review.

Leigh syndrome: One disorder, more than 75 monogenic causes.

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1115-1120

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scholarly article

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10.1080/24701394.2017.1413365

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P433

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P478

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Inna Inashkina

Dita Pelnena

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2017-12-12T00:00:00Z

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29228836

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