1.
Eur J Hum Genet
; 11(8): 585-9, 2003 Aug.
Artículo
en Inglés
| MEDLINE
| ID: mdl-12891378
RESUMEN
Juvenile hemochromatosis (JH) is a rare autosomal recessive disorder that causes iron overload. In the French Canadian region of Saguenay Lac-Saint-Jean the worldwide largest cohort of JH cases has been identified. Here, we report the mapping of this large cohort of cases to the HFE2 locus on chromosome 1q. A maximum multipoint location score of 7.02 was observed with marker D1S2344. A common ancestral haplotype, showing the presence of a founder effect, was identified. The analysis of recombinants allowed us to confirm the JH candidate region.
Asunto(s)
Mapeo Cromosómico/métodos , Cromosomas Humanos Par 1 , Hemocromatosis/genética , Adulto , Canadá/etnología , Femenino , Ligamiento Genético , Marcadores Genéticos , Haplotipos/genética , Humanos , Escala de Lod , Masculino , Linaje
2.
Haematologica
; 88(7): 824-6, 2003 Jul.
Artículo
en Inglés
| MEDLINE
| ID: mdl-12857562