An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
2016 · European Journal of Human Genetics · 106 citations
https://doi.org/10.1038/ejhg.2016.99
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Anne Kurtenbach is an academic researcher. The author has contributed to research in topics: Retinal Development and Disorders & Semiconductor Quantum Structures and Devices & Visual perception and processing mechanisms. The author has an h-index of 21, co-authored 87 publications.
ORCID: 0000-0002-0241-2039https://doi.org/10.1038/ejhg.2016.99
https://doi.org/10.1038/s41598-020-69952-6
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