Clues to quality of journals
Open Access Policy of Helmholtz Association 2016
CC Licencences
Publication Metrics
Home
Deutsch
New EVA Application
Advanced Search
Browse by ...
Publication overview
Statistics (last 5 years)
OA Publications
Submit Publication
Import publication from...
Report missing publication
Contact persons
Help
Text
Endnote (RIS)
BibTeX |
|
Open Access Gold as soon as Publ. Version/Full Text is submitted to ZB.
Mutationen im ABCA4-Gen in einer Familie mit Stargardtscher Erkrankung und Retinitis pigmentosa (STGD1/RP19).
Klin. Monatsbl. Augenheilkd. 219, 590-596 (2002)
Impact Factor
Scopus SNIP
0.521
0.000
Annotations
Special Publikation
Hide on homepage
Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Morbus Stargardt STGD1 homozygote und compound-heterozygote Mutationen Null-Allel rezessive Retinitis pigmentosa RP19
Language
german
Publication Year
2002
HGF-reported in Year
0
ISSN (print) / ISBN
0023-2165
e-ISSN
1439-3999
Quellenangaben
Volume: 219,
Pages: 590-596
Publisher
Thieme
Reviewing status
Peer reviewed
Institute(s)
CCG Hematopoetic Cell Transplants (IMI-KHZ)
Erfassungsdatum
2002-12-02