Literature DB >> 29871478

Kearns-Sayre syndrome is genetically and phenotypically heterogeneous.

Josef Finsterer1, Sinda Zarrouk-Mahjoub2.   

Abstract

Not available.

Entities:  

Mesh：

Year:  2018        PMID： 29871478     DOI： 10.4081/pmc.2018.193

Source DB:  PubMed          Journal:  Pediatr Med Chir        ISSN： 0391-5387


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  2 in total

Review 1.  Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach.

Authors:  Orlando G Barsottini; José Luiz Pedroso; Carlos Roberto Martins; Marcondes Cavalcante França; Pedro Mangabeira Albernaz
Journal:  Cerebellum       Date:  2019-12       Impact factor: 3.847

2.  Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions.

Authors:  Josef Finsterer
Journal:  Yonsei Med J       Date:  2019-02       Impact factor: 2.759
  2 in total

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