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

Endocrine Regulations - Germany
doi 10.2478/enr-2018-0013
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Walter de Gruyter GmbH

Related search

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

Journal of Clinical Pathology
MedicineForensic MedicinePathology
2008English

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

Medical Express
2014English

Leigh Syndrome

2020English

Hematologically Important Mutations: Shwachman–Diamond Syndrome

Blood Cells, Molecules, and Diseases
Molecular MedicineHematologyMolecular BiologyCell Biology
2008English

Clinical Case of Leigh Syndrome in an Infant

INTERNATIONAL NEUROLOGICAL JOURNAL
2017English

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

Mitochondrion
Molecular MedicineCell BiologyMolecular Biology
2015English

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports
Multidisciplinary
2016English

Identification of Novel Genetic Causes of Rett Syndrome-Likephenotypes

Journal of Medical Genetics
Genetics
2016English

Mitochondrial DNA-associated Leigh Syndrome

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy