A Case with NADPHX Dehydratase Deficiency: A Newly Defined Mutation in a Novel Neurodegenerative Disorder

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ÖZ TUNÇER G., RANDA N. C., AYDIN S., AKSOY A.

International Symposium on Genetic Role of Neurometabolic Diseases with Infantile Epilepsy, Taipei, Taiwan, 22 October 2021, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• City: Taipei
• Country: Taiwan
• Ondokuz Mayıs University Affiliated: Yes