Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
Kallio SP; Jakkula E; Purcell S; Suvela M; Koivisto K; Tienari PJ; Elovaara I; Pirttilä T; Reunanen M; Bronnikov D; Viander M; Meri S; Hillert J; Lundmark F; Harbo HF; Lorentzen AR; De Jager PL; Daly MJ; Hafler DA; Palotie A; Peltonen L; Saarela J; Human Molecular Genetics, 2009, vol. 18, issue 9, p 1670, ISSN 14602083. ISBN 14602083.

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