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首页> 外文期刊>European journal of human genetics: EJHG >Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetrance.
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Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetrance.

机译:荷兰家庭中的肿瘤坏死因子受体相关的周期性综合征(TRAPS):TNFRSF1A突变的外显率降低的证据。

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摘要

Mutations of the tumor necrosis factor receptor 1 (TNFRSF1A) gene underly susceptibility to a subset of autosomal dominant recurrent fevers (ADRFs). We report on a two-generation six-member Dutch family in which a novel R92P mutation and reduced plasma TNFRSF1A levels were found in all the children, including two who are unaffected. However, only the daughter proband and father exhibited a typical TNF-receptor associated periodic syndrome (TRAPS) phenotype. PCR-RFLP analysis revealed that the mutation was not present in 120 control chromosomes from unaffected Dutch individuals. As this R92P mutation is present in two unaffected carriers it appears to be less penetrant than previously reported TNFRSF1A mutations involving cysteine residues in the extracellular domains.
机译:肿瘤坏死因子受体1(TNFRSF1A)基因的突变对常染色体显性复发性发烧(ADRFs)的亚群易感。我们报告了一个两代六人荷兰家庭,其中所有儿童中都发现了新的R92P突变和血浆TNFRSF1A水平降低,其中包括两个未受影响的儿童。但是,只有前妻的女儿和父亲才表现出典型的TNF受体相关的周期性综合征(TRAPS)表型。 PCR-RFLP分析表明,该突变在未受影响的荷兰人的120条对照染色体中不存在。由于此R92P突变存在于两个未受影响的载体中,因此它的渗透性似乎不如先前报道的涉及胞外域中半胱氨酸残基的TNFRSF1A突变。

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