Literature DB >> 26566910

Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion.

Michelangelo Mancuso1, Daniele Orsucci2, Corrado Angelini3, Enrico Bertini4, Valerio Carelli5, Giacomo Pietro Comi6, Maria Alice Donati7, Antonio Federico8, Carlo Minetti9, Maurizio Moggio10, Tiziana Mongini11, Filippo Maria Santorelli12, Serenella Servidei13, Paola Tonin14, Antonio Toscano15, Claudio Bruno9, Luca Bello3, Elena Caldarazzo Ienco2, Elena Cardaioli8, Michela Catteruccia4, Paola Da Pozzo8, Massimiliano Filosto16, Costanza Lamperti17, Isabella Moroni18, Olimpia Musumeci15, Elena Pegoraro3, Dario Ronchi6, Donato Sauchelli13, Mauro Scarpelli14, Monica Sciacco10, Maria Lucia Valentino5, Liliana Vercelli11, Massimo Zeviani17, Gabriele Siciliano2.   

Abstract

Mesh:

Substances:

Year:  2015        PMID: 26566910     DOI: 10.1007/s00415-015-7943-9

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


× No keyword cloud information.
  1 in total

1.  MELAS and Kearns-Sayre overlap syndrome due to the mtDNA m. A3243G mutation and large-scale mtDNA deletions.

Authors:  Nian Yu; Yan-Fang Zhang; Kang Zhang; Yuan Xie; Xing-Jian Lin; Qing Di
Journal:  eNeurologicalSci       Date:  2016-04-25
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.