Welcome to my group. My son has a splice site mutation. I met a family at the conference in Baltimore that has a splice site mutation. I created this group for not only me/my son but for anyone else who has a splice site mutation to have a place to talk to oneanother. Hope this group is helpful. I don't proclaim to have answers I just want a group where we could all come together & talk about things that are on our mind. God Bless, Suzanne
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