Literature DB >> 10528258

Expansion of a 27 CAG repeat allele into a symptomatic huntington disease-producing allele.

T E Kelly, P Allinson, R C McGlennen, J Baker, Y Bao.   

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Year:  1999        PMID： 10528258

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  2 in total

1.  De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype.

Authors:  Gunnar Houge; Ove Bruland; Inga Bjørnevoll; Michael R Hayden; Alicia Semaka
Journal:  Neurology       Date:  2013-08-14       Impact factor: 9.910

2.  Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications.

Authors:  D Brocklebank; J Gayán; J M Andresen; S A Roberts; A B Young; S R Snodgrass; J B Penney; M A Ramos-Arroyo; J J Cha; H D Rosas; S M Hersch; A Feigin; S S Cherny; N S Wexler; D E Housman; L R Cardon
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-04-05       Impact factor: 3.568
  2 in total

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