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SYNDROME PEARSON [1 record]

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Record 1 2010-04-13

English

Subject field(s)
  • Genetics
CONT

McShane MA, Hammans SR, Sweeney M, Holt IJ et al. Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. Am J, Hum Genet 48: 39 (1991) Abstract.

French

Domaine(s)
  • Génétique
DEF

Pancytopénie de la première enfance avec insuffisance pancréatique.

Spanish

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