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Am J Hum Genet. 2007 Mar;80(3):478-84. Epub 2007 Jan 10.

Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation.

Author information

  • 1Department of Pediatrics, Paracelsus Private Medical University, Salzburg, Austria. h.mayr@salk.at

Abstract

The mitochondrial phosphate carrier SLC25A3 transports inorganic phosphate into the mitochondrial matrix, which is essential for the aerobic synthesis of adenosine triphosphate (ATP). We identified a homozygous mutation--c.215G-->A (p.Gly72Glu)--in the alternatively spliced exon 3A of this enzyme in two siblings with lactic acidosis, hypertrophic cardiomyopathy, and muscular hypotonia who died within the 1st year of life. Functional investigation of intact mitochondria showed a deficiency of ATP synthesis in muscle but not in fibroblasts, which correlated with the tissue-specific expression of exon 3A in muscle versus exon 3B in fibroblasts. The enzyme defect was confirmed by complementation analysis in yeast. This is the first report of patients with mitochondrial phosphate-carrier deficiency.

PMID:
17273968
[PubMed - indexed for MEDLINE]
PMCID:
PMC1821108
Free PMC Article

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