Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Eriksson M; Brown WT; Gordon LB; Glynn MW; Singer J; Scott L; Erdos MR; Robbins CM; Moses TY; Berglund P; Dutra A; Pak E; Durkin S; Csoka AB; Boehnke M; Glover TW; Collins FS; Nature, 2003, vol. 423, issue 6937, p 293, ISSN 00280836. ISBN 00280836.

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