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Paper Details

Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome.
Mol Genet Genomic Med
20
2014
USH2A, Usher, Usher genes, Usher syndrome, autosomal recessive disorder, blindness, deafness, exon deletions, exons, gene panel, in silico gene panel, modifier gene, patients, whole exon deletions
Author NameAffiliation
Peter M KrawitzInstitute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin Berlin
Ulrike Kr??gerInstitute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin Berlin
Peter N RobinsonInstitute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin Berlin
Peter N RobinsonInstitute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin Berlin
Stefan MundlosInstitute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin Berlin
Jochen HechtBerlin Brandenburg Center for Regenerative Therapies BCRT Berlin
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