Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter

被引:125
作者
Jackson, AP
McHale, DP
Campbell, DA
Jafri, H
Rashid, Y
Mannan, J
Karbani, G
Corry, P
Levene, MI
Mueller, RF
Markham, AF
Lench, NJ
Woods, CG
机构
[1] Univ Leeds, St James Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, Dept Clin Genet, Leeds, W Yorkshire, England
[3] Gen Infirm, Dept Paediat, Leeds, W Yorkshire, England
[4] Fatima Jinnah Med Coll, Lahore, Pakistan
[5] Rawalpindi Med Coll, Rawalpindi, Pakistan
[6] St Lukes Hosp, Dept Paediat, Bradford BD5 0NA, W Yorkshire, England
基金
英国惠康基金;
关键词
D O I
10.1086/301966
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Primary (or "true") microcephaly is inherited as an autosomal recessive trait and is thought to be genetically heterogeneous. Using autozygosity mapping, we have identified a genetic locus (MCPH1) for primary microcephaly, at chromosome 8p22-pter, in two consanguineous families of Pakistani origin. Our results indicate that the gene lies within a 13-cM region between the markers D8S1824 and D8S1825 (maximum multipoint LOD score of 8.1 at D8S277). In addition, we have demonstrated the genetic heterogeneity of this condition by analyzing a total of nine consanguineous families with primary microcephaly.
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页码:541 / 546
页数:6
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