Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene.

Juvenile retinoschisis (RS) is an X linked recessive vitreoretinal disorder for which the basic molecular defect is unknown. The gene for RS has been previously localised by linkage analysis to Xp22.1-p22.2 and the locus order Xpter-DXS16-(DXS43, DXS207)-RS-DXS274-DXS41-Xcen established. To improve...

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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Oudet, C, Weber, C, Kaplan, J, Segues, B, Croquette, M F, Roman, E O, Hanauer, A
Format: Artigo
Langue:Inglês
Publié: 1993
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016337/
https://ncbi.nlm.nih.gov/pubmed/8487275
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