Animal Genetics · 2003 · 18 citations · 20 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeurogeneticsCochlear DisordersGene MappingGenetic DisordersDeafness IdentificationGenetic Inner Ear DisordersHomeotic Gene RegulationHomeotic MutationsMelanocyte BiologyMelanocyte MigrationMultipoint Linkage AnalysisRegulatory Domains
The causative mutation in a gene related to hearing loss in Dalmatians has been elusive. Because of its role in melanocyte migration and differentiation as integral component of the inner ear, we hypothesized that the canine PAX3 (paired box homeotic gene 3) gene could be a candidate for Dalmatian deafness. Therefore, we isolated the canine PAX3 gene and searched for causative mutations within the coding region of important regulatory domains of PAX3. However, no mutations were identified when comparing the DNA sequences of healthy and affected dogs. These results were confirmed by a two-point linkage analysis in 203 Dalmatians transmitting deafness. Our data clearly show that the canine PAX3 gene can be excluded as candidate for Dalmatian deafness.
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Construction of multilocus genetic linkage maps in humans.
E S Lander, P Green · Proceedings of the National Academy of Sciences · 1987 · 1.5K citations · Full text
Life Sciences, Biology, Genetics +14
Faster sequential genetic linkage computations.
Robert W. Cottingham, Ramana M. Idury, Alejandro A. Schäffer · PubMed · 1993 · 1.4K citations