Enzyme Histochemical Assessment of Mitochondrial Functions in Patients with Myopathic form of Limb-Girdle Syndrome

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Enzyme Histochemical Assessment of Mitochondrial Functions in Patients with Myopathic form of Limb-Girdle Syndrome

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wetenschappelijk artikel

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наукова стаття, опублікована у 2011

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Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

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Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

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Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

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Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

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Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

@en

Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

@nl

P1476

Enzyme Histochemical Assessmen ...... c form of Limb-Girdle Syndrome

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P2093

Lily Pal

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Rakesh Pandey

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Ritu Verma

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Vimal Kumar Paliwal

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P2860

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

Adult-onset mitochondrial myopathy

Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients.

Clinical features, investigation, and management of patients with defects of mitochondrial DNA.

A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion.

Pure myopathy associated with a novel mitochondrial tRNA gene mutation.

Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.

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1-8

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scholarly article

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10.5402/2011/204940

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P478

2011

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2011-01-01T00:00:00Z

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P921

mitochondrion