Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Issue 2 (2nd February 2004)

Record Type:: Journal Article
Title:: Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype. Issue 2 (2nd February 2004)
Main Title:: Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype
Authors:: Tonini, M M O
Pavanello, R C M
Gurgel-Giannetti, J
Lemmers, R J
van der Maarel, S M
Frants, R R
Zatz, M
Abstract:
Is Part Of:: Journal of medical genetics. Volume 41:Issue 2(2004)
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 2(2004)
Issue Display:: Volume 41, Issue 2 (2004)
Year:: 2004
Volume:: 41
Issue:: 2
Issue Sort Value:: 2004-0041-0002-0000
Page Start:: e17
Page End:: e17
Publication Date:: 2004-02-02
Subjects:: asymptomatic carriers -- FSHD -- homozygosity
CK, creatinine kinase -- FSHD, facioscapulohumeral muscular dystrophy -- HD, Huntington's disease -- PFGE, pulsed field gel electrophoresis
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.2003.010637 ↗
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:: 18206.xml