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Genotype-based databases for variants causing rare diseases.
Lanthaler B, Wieser S, Deutschmann A, Schossig A, Fauth C, Zschocke J, Witsch-Baumgartner M. Lanthaler B, et al. Among authors: wieser s. Gene. 2014 Oct 15;550(1):136-40. doi: 10.1016/j.gene.2014.08.016. Epub 2014 Aug 8. Gene. 2014. PMID: 25111118
PIK3R1 mutations in SHORT syndrome.
Schroeder C, Riess A, Bonin M, Bauer P, Riess O, Döbler-Neumann M, Wieser S, Moog U, Tzschach A. Schroeder C, et al. Among authors: wieser s. Clin Genet. 2014 Sep;86(3):292-4. doi: 10.1111/cge.12263. Epub 2013 Oct 17. Clin Genet. 2014. PMID: 23980586
163 results