Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
Maria Eriksson(New York State Office for People With Developmental Disabilities), W. Ted Brown(New York State Office for People With Developmental Disabilities), Leslie B. Gordon(Tufts University), Michael W. Glynn(National Institutes of Health), Joel I. Singer(University of Michigan–Ann Arbor), Laura J. Scott(University of Michigan–Ann Arbor), Michael R. Erdos(National Institutes of Health), Christiane M. Robbins(National Human Genome Research Institute), Tracy Moses(National Human Genome Research Institute), Peter Berglund(National Human Genome Research Institute), Amalia Dutra(National Institutes of Health), Evgenia Pak(National Institutes of Health), Sandra G. Durkin(National Human Genome Research Institute), Antonei B. Csòka(Brown University), Michael Boehnke(University of Michigan–Ann Arbor), Thomas W. Glover(National Institutes of Health), Francis S. Collins(National Human Genome Research Institute)
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