Literature DB >> 11102991

Identification of a novel T398A mutation in the ND5 subunit of the mitochondrial complex I and of three novel mtDNA polymorphisms in two patients presenting ocular symptoms.

C Batandier1, A Picard, N Tessier, J Lunardi.   

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Year:  2000        PMID： 11102991     DOI： 10.1002/1098-1004(200012)16:6<532::AID-HUMU19>3.0.CO;2-P

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  3 in total

Review 1.  Eukaryotic complex I: functional diversity and experimental systems to unravel the assembly process.

Authors:  Claire Remacle; M Rosario Barbieri; Pierre Cardol; Patrice P Hamel
Journal:  Mol Genet Genomics       Date:  2008-06-18       Impact factor: 3.291

2.  Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside.

Authors:  Rajeshwari D Koilkonda; John Guy
Journal:  J Ophthalmol       Date:  2010-12-26       Impact factor: 1.909

3.  Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.

Authors:  Ashok Patowary; Ryan Nesbitt; Marilyn Archer; Raphael Bernier; Zoran Brkanac
Journal:  Autism Res       Date:  2017-04-17       Impact factor: 5.216
  3 in total

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