Literature DB >> 8192709

mtDNA in congenital myotonic dystrophy.

D Thyagarajan, E Byrne, A S Noer, P Lertrit, R Kapsa, S Marzuki.   

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Year:  1993        PMID： 8192709      PMCID： PMC1682113     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  12 in total

1.  Unstable DNA sequence in myotonic dystrophy.

Authors:  H G Harley; S A Rundle; W Reardon; J Myring; S Crow; J D Brook; P S Harper; D J Shaw
Journal:  Lancet       Date:  1992-05-09       Impact factor: 79.321

2.  Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.

Authors:  V Cormier; A Rotig; M Tardieu; M Colonna; J M Saudubray; A Munnich
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

3.  "Ragged-red" fibres in myotonic dystrophy.

Authors:  S Ono; H Kurisaki; K Inouye; T Mannen
Journal:  J Neurol Sci       Date:  1986-07       Impact factor: 3.181

4.  An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.

Authors:  M Zeviani; S Servidei; C Gellera; E Bertini; S DiMauro; S DiDonato
Journal:  Nature       Date:  1989-05-25       Impact factor: 49.962

5.  Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Authors:  J M Shoffner; M T Lott; A M Lezza; P Seibel; S W Ballinger; D C Wallace
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

6.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors:  D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

7.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

8.  Focal cytochrome c oxidase deficiency in various neuromuscular diseases.

Authors:  M Yamamoto; Y Koga; E Ohtaki; I Nonaka
Journal:  J Neurol Sci       Date:  1989-06       Impact factor: 3.181

9.  Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.

Authors:  H G Harley; J D Brook; S A Rundle; S Crow; W Reardon; A J Buckler; P S Harper; D E Housman; D J Shaw
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

10.  Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.

Authors:  J Buxton; P Shelbourne; J Davies; C Jones; T Van Tongeren; C Aslanidis; P de Jong; G Jansen; M Anvret; B Riley
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962
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  1 in total

1.  Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy.

Authors:  J Poulton; H G Harley; J Dasmahapatra; G K Brown; C G Potter; B Sykes
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318
  1 in total

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