Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Oshima J, Yu CE, Piussan C, Klein G, Jabkowski J, Balci S, Miki T, Nakura J, Ogihara T, Ells J, Smith M, Melaragno MI, Fraccaro M, Scappaticci S, Matthews J, Ouais S, Jarzebowicz A, Schellenberg GD, Martin GM.
Oshima J, et al. Among authors: schellenberg gd.
Hum Mol Genet. 1996 Dec;5(12):1909-13. doi: 10.1093/hmg/5.12.1909.
Hum Mol Genet. 1996.
PMID: 8968742