Literature DB >> 1895157

Discordance for late-onset degenerative ataxia in monozygous triplets.

A E Harding, T Sura, P Tippett, A M Boughey, J P Patten.   

Abstract

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Year:  1991        PMID： 1895157     DOI： 10.1007/bf00314790

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  3 in total

1.  Characterization of a panel of highly variable minisatellites cloned from human DNA.

Authors:  Z Wong; V Wilson; I Patel; S Povey; A J Jeffreys
Journal:  Ann Hum Genet       Date:  1987-10       Impact factor: 1.670

2.  Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.

Authors:  K Hsiao; H F Baker; T J Crow; M Poulter; F Owen; J D Terwilliger; D Westaway; J Ott; S B Prusiner
Journal:  Nature       Date:  1989-03-23       Impact factor: 49.962

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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