Literature DB >> 12491933

Analysis of human mitochondrial DNA mutations.

Antonio L Andreu1, Ramon Martí, Michio Hirano.   

Abstract

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Year:  2003        PMID： 12491933     DOI： 10.1385/1-59259-330-5:185

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN： 1064-3745


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  2 in total

1.  A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease.

Authors:  Massimiliano Filosto; Gaetana Lanzi; Claudia Nesti; Valentina Vielmi; Eleonora Marchina; Anna Galvagni; Silvia Giliani; Filippo M Santorelli; Alessandro Padovani
Journal:  Mol Genet Metab Rep       Date:  2016-02-27

2.  Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS Patient.

Authors:  Mauro Scarpelli; Francesca Zappini; Massimiliano Filosto; Anna Russignan; Paola Tonin; Giuliano Tomelleri
Journal:  Genet Res Int       Date:  2012-02-20
  2 in total

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