Literature DB >> 6447211

Huntington's disease in two New Britain families.

E M Scrimgeour.   

Abstract

In East New Britain, Papua New Guinea, two Melanesian families were studied in which the typical features of Hungtington's disease were observed in clinically affected members. Mendelian autosomal dominant inheritance was indicated by the respective family trees.

Entities:  

Mesh：

Year:  1980        PMID： 6447211      PMCID： PMC1048547          DOI： 10.1136/jmg.17.3.197

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


  4 in total

1.  Huntington's chorea in Michigan. 2. Selection and mutation.

Authors:  T E REED; J V NEEL
Journal:  Am J Hum Genet       Date:  1959-06       Impact factor: 11.025

2.  Huntington's chorea in Michigan. I. Demography and genetics.

Authors:  T E REED; J H CHANDLER
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

3.  Treatment of Huntington's chorea with isoniazid.

Authors:  T L Perry; P M MacLeod; S Hansen
Journal:  N Engl J Med       Date:  1977-10-13       Impact factor: 91.245

4.  Some problems in Huntington's chorea.

Authors:  D Cameron; G A Venters
Journal:  Scott Med J       Date:  1967-04       Impact factor: 0.729
  4 in total
  4 in total

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

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

Review 2.  Huntington disease: genetics and epidemiology.

Authors:  P M Conneally
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

Review 3.  The epidemiology of Huntington's disease.

Authors:  P S Harper
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

4.  Huntington's disease and leprosy in a New Guinea Highlander.

Authors:  E M Scrimgeour
Journal:  J Med Genet       Date:  1983-12       Impact factor: 6.318
  4 in total

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