Literature DB >> 31625254

Late-onset Leigh syndrome with m.9176T>C mutation in the mitochondrial ATPase 6 gene.

Kazushi Ichikawa1, Yu Tsuyusaki1, Hiroko Shimbo2, Tomohide Goto1.   

Abstract

Entities:  

Keywords:  ATPase 6; Leigh syndrome; mitochondrial DNA; ophthalmoplegia; ptosis

Mesh：

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Year:  2019        PMID： 31625254     DOI： 10.1111/ped.13991

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  2 in total

1.  Leigh Syndrome Mimicking Wernicke's Encephalopathy: A Case Report.

Authors:  Jisoo Oh; Jinok Choi; Soojung Kim; Eun-Ae Yoo
Journal:  Taehan Yongsang Uihakhoe Chi       Date:  2020-09-01

Review 2.  Mitochondrial protein dysfunction in pathogenesis of neurological diseases.

Authors:  Liang Wang; Ziyun Yang; Xiumei He; Shiming Pu; Cheng Yang; Qiong Wu; Zuping Zhou; Xiaobo Cen; Hongxia Zhao
Journal:  Front Mol Neurosci       Date:  2022-09-07       Impact factor: 6.261
  2 in total

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