Name:NTCC? NA25291 LCL DNACategory分類:DNACat#貨號(hào):NTCC?-Coriell NA25291Size/Quantity數(shù)量: 1 VialBiosafety Level生物安全級(jí)別:1Shipping Info運(yùn)輸方式: RTStorage儲(chǔ)存方式: 4CSpecies物種來源: Age年齡: 4 YRGender性別: MaleDescription描述: DOPAMINE TRANSPORTER DEFICIENCY SYNDROME; DTDS | SOLUTE CARRIER FAMILY 6 (NEUROTRANSMITTER TRANSPORTER, DOPAMINE), MEMBER 3; SLC6A3Remarks: Clinically affected; onset of symptoms within the first few weeks after birth; diagnosed at 10 months of age with infantile Parkinsonism and dystonia; DAT1 deficiency; normal head size and growth; cranial nerves: symmetric smile but mild, mask-like facies; atrophy/wasting of temporalis muscles; slightly sunken eyes; no tongue atrophy or fasciculation; continual rapid dystonic contractions of both arms; more static asymmetric dystonic posturing of lower extremities (left flexor bias, right extensor bias); hands often held open, but fisted during opisthotonic episodes; central tone is poor (head lag when pulled to sit, vertical slip-through); tendon reflexes are not increased; left foot in dystonic plantar grasp; no Babinski reflex elicited; cautionary weight gain; severe dysphagia secondary to dystonia; genetic testing by Sanger sequencing; homozygous mutations in SLC6A3 gene; allele 1: 1408T>A and c.1409A>G; allele 2: 1408T>A and c.1409A>G; assistive devices: wheelchair, G-tube feeding.Alternate IDs其他編號(hào): Cell Type細(xì)胞類型:
LCLSource組織來源: LCLGene: SLC6A3 Disease疾病類型: Mutations突變: c.1408T>A c.1409A>GKaryotypes核型: Cytogenetics: Mutation description突變描述: Origin: Transformants: Alias別名: Images圖片:References參考文獻(xiàn):Supplier供應(yīng)商:BioVector質(zhì)粒載體菌株細(xì)胞蛋白抗體基因保藏中心
NTCC典型培養(yǎng)物保藏中心
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