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368. Mitochondrial Complex 1 Deficiency Nuclear Type 4 in a Toddler: A Case Report of NDUFV1 Gene Mutation
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375. Presentation of the Second Case in the World of “Cortıcal Myoclonıc Tremor with Epilepsy, Familial 7”
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376. The Importance of Examination in Febrile Convulsions: Hypotonic Infant Case with Coenzyme Q10 Deficiency
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405. A Unique Case of Subclinical Becker Muscular Dystrophy Due to a Single Exon 48 Deletion in the Dystrophin Gene