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J Pediatr ; 122(3): 419-22, 1993 Mar.
Article de Anglais | MEDLINE | ID: mdl-8095070

RÉSUMÉ

A 6 1/2-year-old girl had developmental regression, and Leigh syndrome was diagnosed. A second girl born to the same mother after heterologous artificial insemination also lost acquired skills and died at 2 1/2 years of age; neuropathologic examination confirmed the diagnosis of Leigh syndrome. Tissues from both children and from the mother had a point mutation at nucleotide 8993 in the adenosinetriphosphatase 6-gene of mitochondrial DNA. This family illustrates that Leigh syndrome can be transmitted by maternal inheritance.


Sujet(s)
ADN mitochondrial/génétique , Maladie de Leigh/génétique , Mutation ponctuelle/génétique , Adenosine triphosphatases/génétique , Enfant , Femelle , Humains , Réaction de polymérisation en chaîne , Polymorphisme de restriction
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