Anzahl der Einträge: 6.
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.
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.
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.
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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