External ophthalmoplegia with severe progressive multiorgan involvement associated with the mtDNA A3243G mutation

Author:

Hansrote Sun,Croul Sidney,Selak Mary,Kalman Bernadette,Schwartzman Robert J.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference22 articles.

1. Progressive external ophthalmoplegia of mitochondrial origin;Laforet;Rev. Neurol.,1997

2. Nucleus-driven multiple large scale deletions of the human mitochondrial genome: a new autosomal dominant disease;Zeviani;Am. J. Hum. Genet.,1990

3. Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism;Melberg;Muscle Nerve,1996

4. Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy;Bohlega;Neurology,1996

5. A case of mitochondrial encephalomyopathy showing ophthalmoplegia, diabetes mellitus and hearing loss associated with the A3243G mutation of mitochondrial DNA;Hoshino;Clin. Neurol.,1997

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