Mitochondrial Complex II Deficiency: Types 1–4
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_423-1
Reference7 articles.
1. Alston CL et al (2012) Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. J Med Genet 49(9):569
2. Fullerton M et al (2020) The genetic basis of isolated mitochondrial complex II deficiency. Mol Genet Metab 131(1–2):53–65
3. Jackson CB et al (2013) Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency. J Med Genet 0:1–6
4. Jain-Ghai S et al (2013) Complex II deficiency – a case report and review of the literature. Am J Med Genet A 161(2):285–294
5. Ma Y-Y et al (2014) Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy. Brain Dev 36(5):394–398
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