Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
about
Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.A novel mitochondrial tRNA(Val) T1658C mutation identified in a CPEO family.Diagnosis and treatment of mitochondrial myopathiesMitochondrial DNA abnormalities in ophthalmological disease.Mitochondrial myopathy: a rare cause of early-onset vocal fold atrophyProgressive External Ophthalmoplegia.
P2860
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
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name
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@en
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@nl
type
label
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@en
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@nl
prefLabel
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@en
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@nl
P2093
P356
P1433
P1476
Ophthalmoplegia due to mitochondrial DNA disease: the need for genetic diagnosis.
@en
P2093
Andrew M Schaefer
Douglass M Turnbull
Philip G Griffiths
Robert W Taylor
P304
P356
10.1002/MUS.20319
P577
2005-07-01T00:00:00Z