I agree that this site is using cookies. You can find further informations
here
.
X
Login
Merkliste (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
zur Desktop-Version
Toggle navigation
Merkliste
1 Ergebnisse
1
A Homologous Genetic Basis of the Murine cpfl1 Mutant and H..:
Chang, Bo
;
Grau, Tanja
;
Dangel, Susann
...
Proceedings of the National Academy of Sciences of the United States of America. 106 (2009) 46 - p. 19581-19586 , 2009
Link:
https://www.jstor.org/stable/25593235
RT Journal T1
A Homologous Genetic Basis of the Murine cpfl1 Mutant and Human Achromatopsia Linked to Mutations in the PDE6C Gene
UL https://suche.suub.uni-bremen.de/peid=jstor-25593235&Exemplar=1&LAN=DE A1 Chang, Bo A1 Grau, Tanja A1 Dangel, Susann A1 Hurd, Ron A1 Jurklies, Bernhard A1 Sener, E. Cumhur A1 Andreasson, Sten A1 Dollfus, Helene A1 Baumann, Britta A1 Bolz, Sylvia A1 Artemyev, Nikolai A1 Kohl, Susanne A1 Heckenlively, John A1 Wissinger, Bernd PB National Academy of Sciences YR 2009 SN 0027-8424 SN 1091-6490 K1 cone photoreceptor K1 hereditary retinal disorder K1 phosphodiesterase K1 Biological sciences K1 Biology K1 Genetics K1 Population genetics K1 Genetic variation K1 Genetic mutation K1 Health sciences K1 Medical conditions K1 Disorders K1 Physical disorders K1 Eye disorders K1 Vision disorders K1 Color vision defects K1 Cytology K1 Cell biology K1 Cells K1 Cellular receptors K1 Sensory receptor cells K1 Photoreceptors K1 Retinal cones K1 Molecular genetics K1 Gene structures K1 Exons K1 Physical sciences K1 Chemistry K1 Chemical compounds K1 Chemicals K1 Acids K1 Nucleic acids K1 DNA K1 Single stranded DNA K1 Complementary DNA K1 Zoology K1 Animals K1 Mammals K1 Rodents K1 Mice K1 Anatomy K1 Body regions K1 Head K1 Eyes K1 Retina K1 Introns JF Proceedings of the National Academy of Sciences of the United States of America VO 106 IS 46 SP 19581 OP 19586 LK http://dx.doi.org/https://www.jstor.org/stable/25593235 DO https://www.jstor.org/stable/25593235 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)