p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria-Reference-Cited by-同舟云学术

p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria

Published:2004-12-27 Issue:1 Volume:57 Page:148-151
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Kirschner Janbernd,Brune Thomas,Wehnert Manfred,Denecke Jonas,Wasner Christina,Feuer Anja,Marquardt Thorsten,Ketelsen Uwe-Peter,Wieacker Peter,Bönnemann Carsten G.,Korinthenberg Rudolf

Funder

German Research Foundation

Pew Scholarship in the Biomedical Sciences

German ministry of education and research (BMBF, Bonn, Germany)

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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4. LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090);Cao;J Hum Genet,2003

5. Positional cloning of the Werner's syndrome gene;Yu;Science,1996

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