Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease

Klara PentelenyiInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary and

Viktoria RemenyiInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary and

Aniko GalInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary and

Gyorgy Mate MilleyInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary and

Aranka CsoszLaboratory of Archeogenetics, Institute of Archeology, Hungarian Academy of Sciences, Budapest, Hungary

Balazs Gusztav MendeLaboratory of Archeogenetics, Institute of Archeology, Hungarian Academy of Sciences, Budapest, Hungary

Maria Judit MolnarInstitute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary and Correspondence[email protected]

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Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease

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Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease

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