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Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.

Abstract:

The human Xp11.23-p11.22 interval has been implicated in several inherited diseases including Wiskott-Aldrich syndrome; three forms of X-linked hypercalciuric nephrolithiaisis; and the eye disorders retinitis pigmentosa 2, congenital stationary night blindness, and Aland Island eye disease. In constructing YAC contigs spanning Xp11. 23-p11.22, we have previously shown that the region around the synaptophysin (SYP) gene is refractory to cloning in YACs, but highly stable in cosmids. Preliminar...

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Publication status:
Published

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Publisher copy:
10.1006/geno.1997.4941

Authors


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Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Medicine, WTC Human Genetics
Ciccodicola, A More by this author
Desicato, S More by this author
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Journal:
Genomics
Volume:
45
Issue:
2
Pages:
340-347
Publication date:
1997-10-05
DOI:
EISSN:
1089-8646
ISSN:
0888-7543
URN:
uuid:ba9692a5-5b09-4b53-a806-e44cfa80c932
Source identifiers:
36102
Local pid:
pubs:36102

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