[先天性病理患儿血液蛋白质罕见电泳变异体频率的评估]
[Assessment of the frequency of rare electrophoretic variants of blood proteins in children with congenital pathology].
作者信息
Afanas'ev K I, Suskov I I, Altukhov Iu P
出版信息
Tsitol Genet. 1984 Mar-Apr;18(2):129-32.
PMID:6729990
Abstract
The frequency of rare electrophoretic protein variants was studied in children with congenital anomalies. The stated frequency (1.07 X 10(-3] proved to be ten-fold higher than in the control group of newborns (1.09 X 10(-4). This difference was mainly due to rare variants of monomorphic proteins. The data obtained confirm the assumption of a functional importance of monomorphic protein loci.
摘要
对患有先天性异常的儿童中罕见电泳蛋白变体的频率进行了研究。所述频率（1.07×10⁻³）被证明比新生儿对照组（1.09×10⁻⁴）高十倍。这种差异主要归因于单态蛋白的罕见变体。所获得的数据证实了单态蛋白基因座具有功能重要性的假设。
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