Andrea H Nemeth

Summary

Affiliation: University of Oxford
Country: UK

Publications

  1. pmc Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34
    A H Nemeth
    Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, United Kingdom
    Am J Hum Genet 67:1320-6. 2000
  2. ncbi The genetics of primary dystonias and related disorders
    Andrea H Nemeth
    The Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Headington, Oxford OX3 7BN, UK
    Brain 125:695-721. 2002

Detail Information

Publications2

  1. pmc Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34
    A H Nemeth
    Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, United Kingdom
    Am J Hum Genet 67:1320-6. 2000
    ..9-cM interval on chromosome 9q34. This work will ultimately allow the disease gene to be identified and its relevance to other types of autosomal recessive cerebellar ataxias to be determined...
  2. ncbi The genetics of primary dystonias and related disorders
    Andrea H Nemeth
    The Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Headington, Oxford OX3 7BN, UK
    Brain 125:695-721. 2002
    ....