Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome. Issue 8 (30th July 2004)

Record Type:: Journal Article
Title:: Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome. Issue 8 (30th July 2004)
Main Title:: Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome
Authors:: Plasilova, M
Chattopadhyay, C
Pal, P
Schaub, N A
Buechner, S A
Mueller, Hj
Miny, P
Ghosh, A
Heinimann, K
Abstract:
Is Part Of:: Journal of medical genetics. Volume 41:Issue 8(2004)
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 8(2004)
Issue Display:: Volume 41, Issue 8 (2004)
Year:: 2004
Volume:: 41
Issue:: 8
Issue Sort Value:: 2004-0041-0008-0000
Page Start:: 609
Page End:: 614
Publication Date:: 2004-07-30
Subjects:: HGPS, Hutchinson-Gilford progeria syndrome -- LMNA, lamin A/C gene -- MAD, mandibuloacral dysplasia
autosomal recessive inheritance -- Hutchinson-Gilford progeria syndrome -- LMNA
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.2004.019661 ↗
Languages:: English
ISSNs:: 1468-6244
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 18072.xml