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                                       Details for article 26 of 157 found articles
 
 
  Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report
 
 
Title: Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report
Author: Ronchi, Dario
Cosi, Alessandra
Tonduti, Davide
Orcesi, Simona
Bordoni, Andreina
Fortunato, Francesco
Rizzuti, Mafalda
Sciacco, Monica
Collotta, Martina
Cagdas, Sophie
Capovilla, Giuseppe
Moggio, Maurizio
Berardinelli, Angela
Veggiotti, Pierangelo
Comi, Giacomo P
Appeared in: BMC neurology
Paging: Volume 11 (2011) nr. 1 pages xx
Year: 2011-07-12
Contents:
Publisher: BioMed Central, London
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 26 of 157 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands