EXOS3 - Whole-exome sequencing of discordant and concordant affected sib pairs in spinocerebellar ataxia 3 (SCA3): a tool to identify novel modifier genes and highlight disrupted molecular pathways is a collaborative research project funded by FCT that brings together Portuguese, Brazilian and United Kingdom's researchers with the aim of identifying genetic modifiers of SCA3, using a whole-exome approach.

EXPLORE THIS WEBPAGE FOR MORE INFORMATION