Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation.
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Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype.Diagnostic evaluation of rhabdomyolysis.Complex-I defect with minimal manifestationsPerspectives on Exertional Rhabdomyolysis.Myopathology of Adult and Paediatric Mitochondrial Diseases.
P2860
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation.
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artigo científico
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bilimsel makale
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scientific article published on 15 February 2011
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Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA
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Recurrent myoglobinuria in a s ...... ndrial DNA tRNA(Ile) mutation.
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type
label
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA
@nl
Recurrent myoglobinuria in a s ...... ndrial DNA tRNA(Ile) mutation.
@en
prefLabel
Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA
@nl
Recurrent myoglobinuria in a s ...... ndrial DNA tRNA(Ile) mutation.
@en
P2093
P2860
P1476
Recurrent myoglobinuria in a s ...... ndrial DNA tRNA(Ile) mutation.
@en
P2093
Evangelia Sotiriou
Katja Heinicke
Kurenai Tanji
Maryam Shirazi
Michio Hirano
Peter E Bosch
Ronald G Haller
Valentina Emmanuele
P2860
P356
10.1016/J.JNS.2011.01.018
P577
2011-02-15T00:00:00Z