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Mitochondrial Complex I Deficiency Associated with Biallelic NDUFA13 Variants Lead to Leigh Syndrome

Author:Kaiyrzhanov, Rauan   Study Group, NDUFA13   

Session Name:P11: Child Neurology and Developmental Neurology: Genetics/Metabolic/Nutritional Disorders 2  

Topic:Child Neurology and Developmental Neurology  

Program Number:P11.008  

Author Institution:South Kazakhstan Medical Academy, Astana, Kazakhstan  International collaborators, Different, United Kingdom