Literature DB >> 10070626

The ND1 T3308C mutation may be a mtDNA polymorphism. Report of two Portuguese patients.

L Vilarinho1, R Chorão, M L Cardoso, H Rocha, C Nogueira, F M Santorelli.   

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Year:  1999        PMID： 10070626     DOI： 10.1023/a:1005471904710

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

Authors:  Y Campos; M A Martín; J C Rubio; M C Gutiérrez del Olmo; A Cabello; J Arenas
Journal:  Biochem Biophys Res Commun       Date:  1997-09-18       Impact factor: 3.575

2.  An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism.

Authors:  R Sakuta; Y Goto; I Nonaka; S Horai
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025
  2 in total
  3 in total

1.  Autism spectrum disorders associated to a deficiency of the enzymes of the mitochondrial respiratory chain.

Authors:  José Guevara-Campos; Lucía González-Guevara; Carmen Puig-Alcaraz; Omar Cauli
Journal:  Metab Brain Dis       Date:  2013-07-10       Impact factor: 3.584

2.  Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic.

Authors:  Qing-Peng Kong; Yong-Gang Yao; Chang Sun; Chun-Ling Zhu; Li Zhong; Cheng-Ye Wang; Wang-Wei Cai; Xiang-Min Xu; An-Long Xu; Ya-Ping Zhang
Journal:  J Hum Genet       Date:  2004-07-22       Impact factor: 3.172

3.  About the "Pathological" role of the mtDNA T3308C mutationellipsis.

Authors:  H Rocha; C Flores; Y Campos; J Arenas; L Vilarinho; F M Santorelli; A Torroni
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025
  3 in total

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