Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
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, Åslaug R.; De Jager, Philip L.; Daly, Mark J.; Hafler, David A.; Palotie, Aarno; Human Molecular Genetics, 2009, vol. 18, issue 9, p 1670, ISSN 09646906. ISBN 14602083.

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