Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.
Eur J Hum Genet
; 8(10): 809-12, 2000 Oct.
Article
en En
| MEDLINE
| ID: mdl-11039585
ABSTRACT
We previously mapped a distinctive autosomal dominant vacuolar neuromyopathy on human chromosome 19p13 in an 8cM region, delimited by D19S209 and D19S177 markers. We now report the fine mapping of the disease locus within an interval of 250 Kb by haplotype analysis performed using a set of 11 novel microsatellite markers isolated from the candidate region.
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Base de datos:
MEDLINE
Asunto principal:
Cromosomas Humanos Par 19
/
Repeticiones de Microsatélite
/
Mapeo Físico de Cromosoma
/
Genes Dominantes
/
Enfermedades Neuromusculares
Idioma:
En
Revista:
Eur J Hum Genet
Asunto de la revista:
GENETICA MEDICA
Año:
2000
Tipo del documento:
Article