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Cite This Article
ÇETİN, Ö. E., YALÇINKAYA, C., ZÜBARİOĞLU, T. (2022). A Rare Leukoencephalopathy: Succinate Dehydrogenase Deficiency. Türk Nöroloji Dergisi, Cilt: 23 - Sayı: 2, 70–72. https://ajindex.com/articles/636864
Journals / Türk Nöroloji Dergisi / 2017 / Cilt: 23 - Sayı: 2
A Rare Leukoencephalopathy: Succinate Dehydrogenase Deficiency
- Journal
- Türk Nöroloji Dergisi
- Pages
- 70–72
- Publication Date
- 2022-11-05
- DOI
- —
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DergiPark Record ↗References (3)
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- Helman G, Caldovic L, Whitehead MT, Simons C, Brockmann K, Edvardson S, Bai R, Moroni I, Taylor JM, Haren KV; SDH Study Group, Taft RJ, Vanderver A, van der Knaap MS. Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy. Ann Neurol 2016;79:379-386
- Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautschi M, Haberli A, Gallati S, Schaller A. Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency. J Med Genet 2014;51:170- 175.