新不列颠两个家族中的亨廷顿舞蹈症
Huntington's disease in two New Britain families.
作者信息
Scrimgeour E M
出版信息
J Med Genet. 1980 Jun;17(3):197-202. doi: 10.1136/jmg.17.3.197.
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.
摘要
在巴布亚新几内亚的东新不列颠省，对两个美拉尼西亚家庭进行了研究，在临床受影响的成员中观察到了亨廷顿舞蹈症的典型特征。各自的家族谱系表明其遗传方式为孟德尔常染色体显性遗传。
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Huntington's chorea in Michigan. I. Demography and genetics.密歇根州的亨廷顿舞蹈症。一、人口统计学与遗传学。
Am J Hum Genet. 1958 Jun;10(2):201-25.
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