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[Starch gel electrophoresis of human blood & ceruloplasmin identification in normal subjects as well as in homozygote & heterozygote subjects for Wilson's disease gene].

作者信息

DE GROUCHY J

出版信息

Rev Fr Etud Clin Biol. 1958 Jun;3(6):621-4.

Abstract
摘要

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引用本文的文献

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A family study of the biochemical defects in Wilson's disease.
J Clin Pathol. 1961 May;14(3):264-70. doi: 10.1136/jcp.14.3.264.
2
DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.
J Clin Invest. 1961 Apr;40(4):707-15. doi: 10.1172/JCI104304.

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