与I型黏多糖贮积症和亨廷顿舞蹈病相关的可变数目串联重复序列的聚合酶链反应 - Suppr

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超能文献

PCR of a VNTR linked to mucopolysaccharidosis type I and Huntington disease.

作者信息

Scott H S, Nelson P V, Hopwood J J, Morris C P

机构信息

Department of Chemical Pathology, Adelaide Children's Hospital, Australia.

出版信息

Nucleic Acids Res. 1991 Nov 25;19(22):6348. doi: 10.1093/nar/19.22.6348-a.

DOI:10.1093/nar/19.22.6348-a

PMID:1835536

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC329172/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c50a/329172/14491b67d2d6/nar00102-0265-a.jpg

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引用本文的文献

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Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele.I型黏多糖贮积症（Hurler综合征）：连锁不平衡表明存在一个主要等位基因。

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本文引用的文献

Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene.与亨廷顿病相关的基因座D4S111被确定为α-L-艾杜糖醛酸酶基因。

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