Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS
利用基因分离株识别罕见疾病变异:5p 染色体上的 C7 变异与多发性硬化症相关
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddp073
Kallio, Suvi P; Jakkula, Eveliina; Purcell, Shaun; Suvela, Minna; Koivisto, Keijo; Tienari, Pentti J; Elovaara, Irina; Pirttilä, Tuula; Reunanen, Mauri; Bronnikov, Denis; Viander, Markku; Meri, Seppo; Hillert, Jan; Lundmark, Frida; Harbo, Hanne F; Lorentzen, Aslaug R; De Jager, Philip L; Daly, Mark J; Hafler, David A; Palotie, Aarno; Peltonen, Leena; Saarela, Janna