The sequences of three cosmids (90 kilobases) from the Huntington's disease region in chromosome 4p16.3 have been determined. A 30,837 base overlap of DNA sequenced from two individuals was found to contain 72 DNA sequence polymorphisms, an average of 2.3 polymorphisms per kilobase (kb). The assembled 58 kb contig contains 62 Alu repeats, and eleven predicted exons representing at least three expressed genes that encode previously unidentified proteins. Each of these genes is associated with a CpG island. The structure of one of the new genes, hda1-1, has been determined by characterizing cDNAs from a placental library. This gene is expressed in a variety of tissues and may encode a novel housekeeping gene
Huntington disease (HD) is an autosomal-dominant disorder of mid-life onset characterized by chorea,...
Huntington disease (HD) is caused by the expansion of a CAG repeat within the coding region of a nov...
Analysis of many families with linked DNA markers has provided support for the Huntington's disease ...
The HD locus has been assigned to 4p16.3 distal to the DNA segment D4S10. However, the precise locat...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The defect causing Huntington disease (HD) has been mapped to 4p16.3, distal to the DNA marker D4S10...
The Huntington’s disease (HD) gene has been mapped in 4~16.3 but has eluded identification. We have ...
The recent observation that the mutation underlying a number of genetic diseases including fragile s...
The incurable neurodegenerative disorder, Huntington's disease (HD), is caused by an expanded, unsta...
IT15 is a novel gene, localized to chromosome 4, and encoding a protein named Huntingtin. A polymorp...
SUMMARY The recent discovery that the gene causing Huntington's disease (HD) resides on chromos...
Two sources of variation in the huntingtin gene, the length of the CCG-rich segment downstream to th...
Huntington disease (HD) is an autosomal-dominant disorder of mid-life onset characterized by chorea,...
Huntington disease (HD) is caused by the expansion of a CAG repeat within the coding region of a nov...
Analysis of many families with linked DNA markers has provided support for the Huntington's disease ...
The HD locus has been assigned to 4p16.3 distal to the DNA segment D4S10. However, the precise locat...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have ...
The defect causing Huntington disease (HD) has been mapped to 4p16.3, distal to the DNA marker D4S10...
The Huntington’s disease (HD) gene has been mapped in 4~16.3 but has eluded identification. We have ...
The recent observation that the mutation underlying a number of genetic diseases including fragile s...
The incurable neurodegenerative disorder, Huntington's disease (HD), is caused by an expanded, unsta...
IT15 is a novel gene, localized to chromosome 4, and encoding a protein named Huntingtin. A polymorp...
SUMMARY The recent discovery that the gene causing Huntington's disease (HD) resides on chromos...
Two sources of variation in the huntingtin gene, the length of the CCG-rich segment downstream to th...
Huntington disease (HD) is an autosomal-dominant disorder of mid-life onset characterized by chorea,...
Huntington disease (HD) is caused by the expansion of a CAG repeat within the coding region of a nov...
Analysis of many families with linked DNA markers has provided support for the Huntington's disease ...