Anzahl der Einträge: 6.
2017
Schulz, H. L.,
Grassmann, F. ,
Kellner, U.,
Spital, G.,
Rüther, K.,
Jägle, H.,
Hufendiek, K.,
Rating, P. und
Weber, Bernhard H. F.
(2017)
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Investigative Ophthalmology & Visual Science (IOVS) 58, S. 394-403.
2009
Stöhr, H.,
Heisig, J. B.,
Benz, P. M.,
Schöberl, S.,
Milenkovic, V. M.,
Strauss, O.,
Aartsen, W.,
Wijnholds, J. ,
Weber, Bernhard H. F. und
Schulz, H. L.
(2009)
TMEM16B, a novel protein with calcium-dependent chloride channel activity, associates with a presynaptic protein complex in photoreceptor terminals.
The Journal of Neuroscience 29 (21), S. 6809-6818.
2002
Schulz, H. L.,
Stöhr, H.,
White, K.,
van Driel, M. A.,
Hoyng, C. B.,
Cremers, F. und
Weber, Bernhard H. F.
(2002)
Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy.
Molecular vision 8, S. 67-71.
2001
2000
Stöhr, H.,
Mah, N.,
Schulz, H. L.,
Gehrig, A.,
Fröhlich, S. und
Weber, Bernhard H. F.
(2000)
EST mining of the UniGene dataset to identify retina-specific genes.
Cytogenetics and cell genetics 91, S. 267-277.
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