Repeat expansions in NOP56 are a cause of spinocerebellar ataxia Type 36 in the British population
NOP56基因的重复扩增是英国人群中36型脊髓小脑性共济失调的病因之一。
期刊:Brain Communications
影响因子:4.5
doi:10.1093/braincomms/fcad244
Lam, Tanya; Rocca, Clarissa; Ibanez, Kristina; Dalmia, Anupriya; Tallman, Samuel; Hadjivassiliou, Marios; Hensiek, Anke; Nemeth, Andrea; Facchini, Stefano; Wood, Nicholas; Cortese, Andrea; Houlden, Henry; Tucci, Arianna