NTCC® NA23652 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA23652
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA23652
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
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Name:NTCC® NA23652 Fibroblast DNACategory分类:DNACat#货号:NTCC®-Coriell NA23652Size/Quantity数量: 1 VialBiosafety Level生物安全级别:1Shipping Info运输方式: RTStorage储存方式: 4CSpecies物种来源: Age年龄: 5 YRGender性别: FemaleDescription描述: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6; MDDGA6 (WALKER-WARBURG SYNDROME INCLUDED) | CHROMOSOME DELETIONRemarks: Clinically affected; decreased alpha dystroglycan; diagnosed by muscle biopsy and muscle imaging (MRI); type II lissencephaly (predominant pachygyria-frontal>occipital); possible polymicrogyria; inferior vermis hypoplasia; small pons; inferior vermis hypoplasia; patchy white matter abnormalities in higher parietal white matter; small tectum; mental retardation; turned in bed without assistance at age 3 months; sat without assistance at age 6 months; walked indoors without assistance at age 2 years; ejection fraction > 60%; donor subject is a compound heterozygote: the paternal allele has a 74 kb deletion {chromosome 22q12.3: [32330175 (SNP rs2239746)]- [32403758 (SNP rs2267255)]} of the LARGE gene including coding exons; the maternal allele has a G>A transition at nucleotide 1525 in exon 13 (1525G>A) resulting in the substitution of lysine for glutamic acid at codon 509 [Glu509Lys (E509K)].Alternate IDs其他编号: Cell Type细胞类型:
FibroblastSource组织来源: FibroblastGene: LARGE Disease疾病类型: Mutations突变: DEL LARGE GLU509LYSKaryotypes核型: Cytogenetics: Mutation description突变描述: Origin: Transformants: Alias别名: Images图片:References参考文献:Supplier供应商:BioVector质粒载体菌株细胞蛋白抗体基因保藏中心
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