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Chromosomal localization of the mouse homolog of the Huntington's disease linked G8 (D4S10) marker.

作者信息

Cheng S V, Gross Lugo T, Tanzi R E, Whitney J B, Fournier R E, Gusella J F

机构信息

Neurogenetics Laboratory, Massachusetts General Hospital, Boston.

出版信息

DNA. 1987 Oct;6(5):401-7. doi: 10.1089/dna.1987.6.401.

Abstract

The human DNA probe G8 defines D4S10, a polymorphic locus tightly linked to the Huntington's disease gene on human chromosome 4. A subclone of G8, pSC33, showed significant cross-hybridization to discrete restriction fragments in total genomic mouse DNA. The probe detected restriction fragment length polymorphisms (RFLPs) with the enzymes Taq I and Msp I, permitting chromosomal localization of the mouse G8 homolog by linkage analysis using three sets of recombinant inbred mouse strains: BXH, BXD, and AKXD. The mouse locus was mapped to the central region of chromosome 11 at 1 centiMorgan from the SPARC gene, a locus whose human counterpart is on human chromosome 5.

摘要

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