Open Access Green as soon as Postprint 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)
Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Morbus Stargardt STGD1 homozygote und compound-heterozygote Mutationen Null-Allel rezessive Retinitis pigmentosa RP19
ISSN (print) / ISBN
0023-2165
e-ISSN
1439-3999
Quellenangaben
Volume: 219,
Pages: 590-596
Publisher
Thieme
Non-patent literature
Publications
Reviewing status
Peer reviewed
Institute(s)
CCG Hematopoetic Cell Transplants (IMI-KHZ)