蛋白质/抗原/多肽 >> 重组蛋白
重组中心体蛋白152
产品介绍 基因名: CEP152 产品别名: MCPH4; MCPH9; SCKL5; CEP152; centrosomal protein 152; centrosomal protein 152; centrosomal protein of 152 kDa; asterless; centrosomal protein 152kDa; microcephaly, primary autosomal recessive 4; 中心体蛋白152; 背景信息: Defects in CEP152 are the cause of microcephaly primary type 4 (MCPH4). A disease defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Affected individuals are mentally retarded. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits due to degenerative brain disorder. 标签:His-tag |
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