Sofia Reyes - FOXP1 community - RareConnect

Sofia Reyes - FOXP1 community - RareConnect

RARECONNECT

Online Communities for Rare Disease Patients The Spanish family of a daughter with a FOXP1 mutation finds RareConnect and shares their story Latest FOXP1 Community Activity FOXP1 gene mutation in the Developmental Brain Disorders Databasereply published 7 days ago show transcript Are you facing difficulties accessing your treatment? Please report them to EURORDIStopic published 26 days ago show transcript FOXP1 in Germanyreply published about 1 month ago show transcript Looking for advicereply published about 1 month ago show transcript Greetings to our newest membersreply published about 1 month ago show transcript Family scours genetic data to identify mutation causing their son's disabilitiestopic published 5 months ago show transcript Exome sequencing grant programtopic published 5 months ago show transcript Technology helps give disorders a nametopic published 5 months ago show transcript