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Publications by Johannes A Mayr

Molecular Diagnosis in Mitochondrial Complex I Deficiency Using Exome Sequencing

Journal of Medical Genetics
Genetics
2012English

Sengers Syndrome: Six Novel AGK Mutations in Seven New Families and Review of the Phenotypic and Mutational Spectrum of 29 Patients

Orphanet Journal of Rare Diseases
MedicineGeneticsPharmacology
2014English

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