Hepatocerebral Mitochondrial DNA Depletion
Two novel homozygous mutations, G352A and C269T, are documented in the gene for deoxyguanosine kinase (DGK) in 3 children with hepatocerebral mitochondrial DNA depletion syndrome reported from Columbia University College of Physicians and Surgeons, New York; University of Pisa, Italy; University of...
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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2005-08-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | Two novel homozygous mutations, G352A and C269T, are documented in the gene for deoxyguanosine kinase (DGK) in 3 children with hepatocerebral mitochondrial DNA depletion syndrome reported from Columbia University College of Physicians and Surgeons, New York; University of Pisa, Italy; University of Toronto, Canada; and University of Melbourne, Australia. |
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| Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-19-8-2 |