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Staley KJ, Sims KB, Grant PE, et al. 
Case records of the Massachusetts General Hospital. Case 28-2008. An 8-day-old infant with congenital deafness, lethargy, and hypothermia. [Case Reports, Clinical Conference, Journal Article]
N Engl J Med 2008 Sep 11; 359(11):1156-67.
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Laird PW, Mohney BG, Renaud DL 
Bull's-eye maculopathy in an infant with Leigh disease. [Case Reports, Journal Article]
Am J Ophthalmol 2006 Jul; 142(1):186-7.
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Nagashima T, Mori M, Katayama K, et al. 
Adult Leigh syndrome with mitochondrial DNA mutation at 8993. [Case Reports, Journal Article, Review]
Acta Neuropathol (Berl) 1999 Apr; 97(4):416-22.
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Rossi A, Biancheri R, Bruno C, et al. 
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings. [Case Reports, Journal Article]
AJNR Am J Neuroradiol 2003 Jun-Jul; 24(6):1188-91.
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Zhang Y, Yang YL, Sun F, et al. 
Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome. [JOURNAL ARTICLE]
J Inherit Metab Dis 2007 Feb 24.
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Tomczak R, Rieber A, Zeitler H, et al. 
[Newborn infant with cerebral symptoms. Leigh disease] [Case Reports, Journal Article]
Radiologe 1996 Jul; 36(7):591-2.
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Coker SB, Thomas C 
Connatal Leigh disease. [Case Reports, Journal Article]
Clin Pediatr (Phila) 1995 Jul; 34(7):349-52.
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[A clinical case of Li syndrome caused by a mitochondrial DNA mutation] [Journal Article]
Zh Nevrol Psikhiatr Im S S Korsakova 2008; 108(5):80-3.
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Absalon MJ, Harding CO, Fain DR, et al. 
Leigh syndrome in an infant resulting from mitochondrial DNA depletion. [Case Reports, Journal Article]
Pediatr Neurol 2001 Jan; 24(1):60-3.
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