Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

By Cao Henian   Hegele Robert A.  

Human Molecular Genetics, Vol. 9, Iss. 1, 2000-01 ,pp. : 109-112

Oxford University Press

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A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features

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Molecular Syndromology, Vol. 1, Iss. 3, 2010-09 ,pp. : 127-132

Karger

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A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

By Lloyd D.J.   Trembath R.C.   Shackleton S.  

Human Molecular Genetics, Vol. 11, Iss. 7, 2002-04 ,pp. : 769-777

Oxford University Press

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Altered pre-lamin A processing is a common mechanism leading to lipodystrophy

By Capanni Cristina  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1489-1502

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Nuclear sequestration of -sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytes

By Heydemann Ahlke   Demonbreun Alexis   Hadhazy Michele   Earley Judy U.   McNally Elizabeth M.  

Human Molecular Genetics, Vol. 16, Iss. 4, 2007-02 ,pp. : 355-363

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