Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation

Author: Verstraeten Valerie L.R.M.   Broers Jos L.V.   van Steensel Maurice A.M.   Zinn-Justin Sophie   Ramaekers Frans C.S.   Steijlen Peter M.   Kamps Miriam   Kuijpers Helma J.H.   Merckx Diane   Smeets Hubert J.M.   Hennekam Raoul C.M.   Marcelis Carlo L.M.   van den Wijngaard Arthur  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.15, Iss.16, 2006-08, pp. : 2509-2522

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content