A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.
Neurology
; 67(5): 900-1, 2006 Sep 12.
Article
en En
| MEDLINE
| ID: mdl-16966564
ABSTRACT
The authors investigated genetic factors contributing to restless legs syndrome (RLS) by performing a 10-cM genome-wide scan in a large French-Canadian pedigree. They detected an autosomal-dominant locus mapping to chromosome 20p13, with a maximum multipoint lod score of 3.86 at marker D20S849. This is the third reported autosomal-dominant locus for RLS and the first autosomal-dominant RLS locus in the French-Canadian population.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Síndrome de las Piernas Inquietas
/
Cromosomas Humanos Par 20
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Salud de la Familia
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Mapeo Cromosómico
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Ligamiento Genético
Límite:
Female
/
Humans
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Male
Idioma:
En
Revista:
Neurology
Año:
2006
Tipo del documento:
Article
País de afiliación:
Canadá