Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele. Issue 7 (1st July 2003)

Record Type:: Journal Article
Title:: Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele. Issue 7 (1st July 2003)
Main Title:: Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
Authors:: Perrault, I
Hanein, S
Gerber, S
Barbet, F
Dufier, J-L
Munnich, A
Rozet, J-M
Kaplan, J
Abstract:
Is Part Of:: Journal of medical genetics. Volume 40:Issue 7(2003)
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 7(2003)
Issue Display:: Volume 40, Issue 7 (2003)
Year:: 2003
Volume:: 40
Issue:: 7
Issue Sort Value:: 2003-0040-0007-0000
Page Start:: e90
Page End:: e90
Publication Date:: 2003-07-01
Subjects:: CRX -- Leber congenital amaurosis -- autosomal dominant -- heterozygous null allele
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.40.7.e90 ↗
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:: 19662.xml