Literature DB >> 2351981

Familial cerebellar ataxia and possible cosegregation with an inversion in chromosome 4.

I D Young, D P Duckett.   

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Year:  1990        PMID： 2351981      PMCID： PMC488072          DOI： 10.1136/jnnp.53.5.441-a

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


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  3 in total

1.  Mapping of mutation causing Friedreich's ataxia to human chromosome 9.

Authors:  S Chamberlain; J Shaw; A Rowland; J Wallis; S South; Y Nakamura; A von Gabain; M Farrall; R Williamson
Journal:  Nature       Date:  1988-07-21       Impact factor: 49.962

2.  Genetic aspects of autosomal dominant late onset cerebellar ataxia.

Authors:  A E Harding
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

3.  The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

Authors:  A E Harding
Journal:  Brain       Date:  1982-03       Impact factor: 13.501
  3 in total

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