Linkage studies in X-linked Alport's syndrome View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1988-12

AUTHORS

S. Szpiro-Tapia, G. Bobrie, M. Guilloud-Bataille, S. Heuertz, C. Julier, J. Frézal, J. P. Grünfeld, M. C. Hors-Cayla

ABSTRACT

Four kindreds segregating for Alport's syndrome (ASLN) compatible with a X-linked inheritance were studied for linkage with polymorphic markers of the human X chromosome. No recombinant was observed between the ASLN locus and the DXS101 and DXS94 loci, the maximum lod scores were z = 3.93 and 3.50 respectively. Linkage data between the ASLN locus and the other genetic markers used in the present study are in keeping with the assignment of the mutation to the proximal Xq arm. More... »

PAGES

85-87

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00283736

DOI

http://dx.doi.org/10.1007/bf00283736

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1049879254

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/2904407


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