Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Eriksson, Maria; Brown, W. Ted; Gordon, Leslie B.; Glynn, Michael W.; Singer, Joel; Scott, Laura; Erdos, Michael R.; Robbins, Christiane M.; Moses, Tracy Y.; Berglund, Peter; Dutra, Amalia; Pak, Evgenia; Durkin, Sandra; Csoka, Antonei B.; Boehnke, Michael; Glover, Thomas W.; Collins, Francis S.; Nature, 2003, vol. 423, issue 6937, p 293, ISSN 00280836. ISBN 00280836.

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