A Gene Map of the Best’s Vitelliform Macular Dystrophy Region in Chromosome 11q12–q13.1

Best’s vitelliform macular dystrophy is an autosomal dominant disorder of unknown causes. To identify the underlying gene defect the disease locus has been mapped to an ∼1.4-Mb region on chromosome 11q12–q13.1. As a prerequisite for its positional cloning we have assembled a high coverage PAC contig...

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Bibliografische gegevens
Gepubliceerd in:Genome Res
Hoofdauteurs: Stöhr, Heidi, Marquardt, Andreas, Rivera, Andrea, Cooper, Paul R., Nowak, Norma J., Shows, Thomas B., Gerhard, Daniela S., Weber, Bernhard H.F.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Cold Spring Harbor Laboratory Press 1998
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Letters
Online toegang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC310689/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9445487/
https://ncbi.nlm.nih.govhttps://doi.org/10.1101/gr.8.1.48
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