Literature DB >> 9279769

Juvenile onset Huntington's disease in an Omani child with asymptomatic, at risk parents.

E M Scrimgeour, R L Koul, P R Chand, J K Tharakan, C A Frew.   

Abstract

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Year:  1997        PMID： 9279769      PMCID： PMC1051042          DOI： 10.1136/jmg.34.8.701

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

Authors:  Y P Goldberg; B Kremer; S E Andrew; J Theilmann; R K Graham; F Squitieri; H Telenius; S Adam; A Sajoo; E Starr
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

2.  Huntington's disease in two unrelated Arab kindreds and in an Afghani family resident in Saudi Arabia.

Authors:  E M Scrimgeour; S A Tahoon; T H Zawawi
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

3.  A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.

Authors:  B Kremer; P Goldberg; S E Andrew; J Theilmann; H Telenius; J Zeisler; F Squitieri; B Lin; A Bassett; E Almqvist
Journal:  N Engl J Med       Date:  1994-05-19       Impact factor: 91.245
  3 in total
  1 in total

1.  Huntington disease (chorea) in the middle East.

Authors:  Euan M Scrimgeour
Journal:  Sultan Qaboos Univ Med J       Date:  2009-03-16
  1 in total

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