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Familial Behr syndrome-like phenotype with autosomal dominant inheritance.
Felicio AC, Godeiro-Junior C, Alberto LG, Pinto AP, Sallum JM, Teive HG, Barsottini OG. Felicio AC, et al. Parkinsonism Relat Disord. 2008;14(4):370-2. doi: 10.1016/j.parkreldis.2007.08.008. Epub 2007 Oct 30. Parkinsonism Relat Disord. 2008. PMID: 17977780
Behr syndrome is an autosomal recessive disease characterized by early-onset ataxia, optic atrophy and other signs such as pyramidal tract dysfunction. ...In this case report we present a family pedigree of patients with an inherited autosomal dominant Behr syndrome …
Behr syndrome is an autosomal recessive disease characterized by early-onset ataxia, optic atrophy and other signs such as pyramidal …
MMR: a tool for read multi-mapper resolution.
Kahles A, Behr J, Rätsch G. Kahles A, et al. Bioinformatics. 2016 Mar 1;32(5):770-2. doi: 10.1093/bioinformatics/btv624. Epub 2015 Oct 30. Bioinformatics. 2016. PMID: 26519503 Free PMC article.
AVAILABILITY AND IMPLEMENTATION: Open source code and documentation are available for download at http://github.com/ratschlab/mmr Comprehensive testing results and further information can be found at http://bioweb.me/mmr. CONTACT: andre.kahles@ratschlab.org or gunnar.ratsc …
AVAILABILITY AND IMPLEMENTATION: Open source code and documentation are available for download at http://github.com/ratschlab/mmr Comprehens …