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Gene rearrangements in the glucocerebrosidase-metaxin region giving rise to disease-causing mutations and polymorphisms.: Analysis of 25 RecNciI alleles in Gaucher disease patients
被引:3
|作者:
Díaz-Font, A
Cormand, B
Blanco, M
Chamoles, N
Chabás, A
Grinberg, D
Vilageliu, L
机构:
[1] Univ Barcelona, Fac Biol, Dept Genet, E-08028 Barcelona, Spain
[2] Fdn Estudio Enfermedades Neurometab, RA-1425 Buenos Aires, DF, Argentina
[3] Hosp Clin Barcelona, Inst Bioquim Clin, Corporacio Sanitaria, E-08028 Barcelona, Spain
关键词:
D O I:
10.1007/s00439-002-0894-0
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
The glucocerebrosidase and metaxin genes lie in a gene-rich region that also includes two corresponding pseudogenes. This gives rise to recombinant alleles. We analysed two groups of patients from Argentina and Spain: 25 bearing the RecNcil allele and 36 carrying L444P. The mutational mechanism is described and the crossover site precisely defined. Most of the RecNcil alleles were generated by gene conversion. Rearranged alleles involving the metaxin gene were also identified. The high frequency of RecNcil alleles associated with a polymorphic rearrangement at the metaxin level is probably due to a founder effect.
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页码:426 / 429
页数:4
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