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  • Author: Ottolenghi C
  • References

Author: Ottolenghi C


References 5 references


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  • Habarou F, et al. (2017) Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy. Am J Hum Genet 101(2):283-290 PMID:28757203
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  • Soreze Y, et al. (2013) Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. Orphanet J Rare Dis 8:192 PMID:24341803
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  • Ottolenghi C, et al. (2000) The genomic structure of c14orf1 is conserved across eukarya. Mamm Genome 11(9):786-8 PMID:10967139
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  • Veitia R and Ottolenghi C (2000) Placing parallel stranded DNA in an evolutionary context. J Theor Biol 206(2):317-22 PMID:10966769
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  • Veitia RA, et al. (1999) A novel human gene, encoding a potential membrane protein conserved from yeast to man, is strongly expressed in testis and cancer cell lines. Cytogenet Cell Genet 85(3-4):217-20 PMID:10449901
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