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一种青少年发病的成年型糖尿病(MODY)基因定位于12号染色体长臂。

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q.

作者信息

Vaxillaire M, Boccio V, Philippi A, Vigouroux C, Terwilliger J, Passa P, Beckmann J S, Velho G, Lathrop G M, Froguel P

机构信息

CNRS EP10, Institut Pasteur de Lille, France.

出版信息

Nat Genet. 1995 Apr;9(4):418-23. doi: 10.1038/ng0495-418.

Abstract

Maturity-onset diabetes of the young (MODY) is a subtype of non-insulin dependent diabetes mellitus, with early age of onset. MODY is genetically heterogeneous, associated with glucokinase mutations and a locus on chromosome 20q; in about 50% of cases, its genetic background is unknown. We have studied 12 families in which MODY is unlinked to either glucokinase or chromosome 20q markers, and find significant evidence for linkage with microsatellite markers on chromosome 12q, most likely within a 7 centimogran interval bracketed by D12S86 and D12S342. The disease was estimated to be linked to this chromosome region in approximately 50% of families in a heterogeneity analysis. These MODY patients exhibit major hyperglycaemia with a severe insulin secretory defect, suggesting that the causal gene is implicated in pancreatic beta-cell function.

摘要

青年发病的成年型糖尿病(MODY)是早发型非胰岛素依赖型糖尿病的一个亚型。MODY具有遗传异质性,与葡萄糖激酶突变及20号染色体上的一个位点相关;约50%的病例其遗传背景尚不清楚。我们研究了12个家族,其中MODY与葡萄糖激酶或20号染色体q臂标记均无连锁关系,并且发现有显著证据表明与12号染色体q臂上的微卫星标记连锁,最有可能位于由D12S86和D12S342界定的7厘摩区间内。在一项异质性分析中,估计约50%的家族中该疾病与这个染色体区域连锁。这些MODY患者表现出严重高血糖并伴有严重的胰岛素分泌缺陷,提示致病基因与胰腺β细胞功能有关。

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