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Publications by Katarina Brennerova

Mutations in SURF1 Are Important Genetic Causes of Leigh Syndrome in Slovak Patients

Endocrine Regulations

English

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Light and Electron Microscopy Characteristics of the Muscle of Patients With SURF1 Gene Mutations Associated With Leigh Disease

Journal of Clinical Pathology

Forensic Medicine

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The Prevalence of Mitochondrial DNA Mutations in Leigh Syndrome in a Brazilian Series

Medical Express

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Leigh Syndrome

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Hematologically Important Mutations: Shwachman–Diamond Syndrome

Blood Cells, Molecules, and Diseases

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Molecular Biology

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Clinical Case of Leigh Syndrome in an Infant

INTERNATIONAL NEUROLOGICAL JOURNAL

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A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome

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Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports

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Identification of Novel Genetic Causes of Rett Syndrome-Likephenotypes

Journal of Medical Genetics

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Mitochondrial DNA-associated Leigh Syndrome

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