Samantha Bryen
Samantha Bryen is a Variant Curator in the Centre for Population Genomics’ Rare Disease Analysis team, focusing on genomic analysis for families with rare diseases, including neuromuscular diagnostics and splicing-variant analysis.
Samantha Bryen is a Variant Curator in the Centre for Population Genomics’ Rare Disease Analysis team, focusing on genomic analysis for families with rare diseases, including neuromuscular diagnostics and splicing-variant analysis.