It seems or looks like my son Francis' mutation is very rare and I wanted to know if anyone elses son might have the same mutation. My sons mutation is:
IVS55-1 or HEMIZYGOUS IVS55-1G>C MUTATION
Maybe I'm grassping at straws, but all of a sudden I am feeling alone again. I just need a little advice and/or help from anyone. Just a little direction. Maybe I will just call the PPMD office.
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