Literature DB >> 9701486

Mitochondrial DNA 8993 T > C mutation presenting as juvenile Leigh syndrome with respiratory failure.

S C Mak1, C S Chi, C R Tsai.   

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Year:  1998        PMID： 9701486     DOI： 10.1177/088307389801300709

Source DB:  PubMed          Journal:  J Child Neurol        ISSN： 0883-0738            Impact factor:   1.987


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  3 in total

1.  Leigh syndrome: serial MR imaging and clinical follow-up.

Authors:  J Arii; Y Tanabe
Journal:  AJNR Am J Neuroradiol       Date:  2000-09       Impact factor: 3.825

2.  A meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations.

Authors:  Xueli Chang; Yaxin Wu; Jie Zhou; Huaxing Meng; Wei Zhang; Junhong Guo
Journal:  Medicine (Baltimore)       Date:  2020-01       Impact factor: 1.889

3.  Leigh Syndrome in Childhood: Neurologic Progression and Functional Outcome.

Authors:  Jin Sook Lee; Hunmin Kim; Byung Chan Lim; Hee Hwang; Jieun Choi; Ki Joong Kim; Yong Seung Hwang; Jong Hee Chae
Journal:  J Clin Neurol       Date:  2016-04       Impact factor: 3.077
  3 in total

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