Literature DB >> 27206685

Significance of rostral brain lesions of Leigh syndrome associated with the mitochondrial DNA 8993T > G mutation.

Yukiko Iida1, Katsunori Fujii2.   

Abstract

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Keywords:  Leigh syndrome; M.8993T>G; Mitochondrial disorder; Rostral distribution

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Year:  2016        PMID： 27206685     DOI： 10.1016/j.jns.2016.05.023

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


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  1 in total

1.  Intractable Epilepsy in Maternally Inherited Leigh Syndrome (MILS) Due to the Sporadic Variant m.8993T>G in MT-ATP6: A Case Report.

Authors:  Josef Finsterer
Journal:  Cureus       Date:  2022-02-28
  1 in total

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