Literature DB >> 8778272

Debrisoquine hydroxylase polymorphism in Leber's hereditary optic neuropathy.

R M Chalmers, O Bandmann, A E Harding.   

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Year:  1996        PMID： 8778272      PMCID： PMC486381          DOI： 10.1136/jnnp.60.5.588

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  5 in total

1.  Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease.

Authors:  C A Smith; A C Gough; P N Leigh; B A Summers; A E Harding; D M Maraganore; S G Sturman; A H Schapira; A C Williams; D M Maranganore
Journal:  Lancet       Date:  1992-06-06       Impact factor: 79.321

2.  X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.

Authors:  X D Bu; J I Rotter
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-15       Impact factor: 11.205

3.  Maternally transmitted histocompatibility antigen of mice: a hydrophobic peptide of a mitochondrially encoded protein.

Authors:  B Loveland; C R Wang; H Yonekawa; E Hermel; K F Lindahl
Journal:  Cell       Date:  1990-03-23       Impact factor: 41.582

4.  Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

Authors:  A E Harding; M G Sweeney; G G Govan; P Riordan-Eva
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

5.  The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation.

Authors:  P Riordan-Eva; M D Sanders; G G Govan; M G Sweeney; J Da Costa; A E Harding
Journal:  Brain       Date:  1995-04       Impact factor: 13.501
  5 in total

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