Andrea H Nemeth
Affiliation: University of Oxford
- Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34A 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...
- The genetics of primary dystonias and related disordersAndrea H Nemeth
The Wellcome Trust Centre for Human Genetics, Roosevelt Drive, Headington, Oxford OX3 7BN, UK
Brain 125:695-721. 2002....