Detection of mtDNA deletion in Pearson syndrome by two independent PCR assays from Guthrie card
Pearson syndrome is a multisystem juvenile condition associated with deletions in the mitochondrial genome. The most common 4977 bp deletion of mitochondrial DNA (mtDNA) can mainly be detected in the patients' peripheral blood. Here we report a child with a clinically unclarified diagnosis wher...
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Veröffentlicht in: | Clinical genetics 1998-03, Vol.53 (3), p.210-213 |
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Sprache: | eng |
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