Anzahl der Publikationen: 4
	Zeitschriftenartikel
    Hytonen, Marjo K.; Sarviaho, Riika; Jackson, Christopher B.; Syrja, Pernilla; Jokinen, Tarja; Matiasek, Kaspar; Rosati, Marco; Dallabona, Cristina; Baruffini, Enrico; Quintero, Ileana; Arumilli, Meharji; Monteuuis, Geoffray; Donner, Jonas; Anttila, Marjukka; Suomalainen, Anu; Bindoff, Laurence A. und Lohi, Hannes
  
(2021):
		In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration.
	
	 In: Human Genetics, Bd. 140, Nr.  11: S. 1593-1609
	
      
        
      
 
    Ng, Yi Shiau; Bindoff, Laurence A.; Gorman, Grainne S.; Klopstock, Thomas; Kornblum, Cornelia; Mancuso, Michelangelo; McFarland, Robert; Sue, Carolyn M.; Suomalainen, Anu; Taylor, Robert W.; Thorburn, David R. und Turnbull, Doug M.
  
(2021):
		Mitochondrial disease in adults: recent advances and future promise.
	
	 In: Lancet Neurology, Bd. 20, Nr.  7: S. 573-584
	
      
        
      
 
    Ng, Yi Shiau; Bindoff, Laurence A.; Gorman, Grainne S.; Klopstock, Thomas; Kornblum, Cornelia; Mancuso, Michelangelo; McFarland, Robert; Sue, Carolyn M.; Suomalainen, Anu; Taylor, Robert W.; Thorburn, David R. und Turnbull, Doug M.
  
(2021):
		Mitochondrial disease in adults: recent advances and future promise.
	
	 In: Lancet Neurology, Bd. 20, Nr.  7: S. 573-584
	
      
        
      
 
    Haack, Tobias B.; Ignatius, Erika; Calvo-Garrido, Javier; Iuso, Arcangela; Isohanni, Pirjo; Maffezzini, Camilla; Lönnqvist, Tuula; Suomalainen, Anu; Gorza, Matteo; Kremer, Laura S.; Graf, Elisabeth; Hartig, Monika; Berutti, Riccardo; Paucar, Martin; Svenningsson, Per; Stranneheim, Henrik; Brandberg, Göran; Wedell, Anna; Kurian, Manju A.; Hayflick, Susan A.; Venco, Paola; Tiranti, Valeria; Strom, Tim M.; Dichgans, Martin; Horvath, Rita; Holinski-Feder, Elke; Freyer, Christoph; Meitinger, Thomas; Prokisch, Holger; Senderek, Jan; Wredenberg, Anna; Carroll, Christopher J. und Klopstock, Thomas
  
(2016):
		Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.
	
	 In: American Journal of Human Genetics, Bd. 99, Nr.  3: S. 735-743
	
      
        
      
 
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