Cystic Fibrosis Forum (EXP)

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  1. L

    rare mutation!!! c.4375-20A>G.

    Dear Mrs. Campos, I am familiar with 4375-20A>G (c.4243-20A>G) and think that it is likely a benign sequence change and, if no symptoms now, your baby does not have cystic fibrosis. Why? It is far within an intron (non-protein coding region) and it has been detected in 0.2% of 1990 NORMAL...
  2. L

    rare mutation!!! c.4375-20A>G.

    Dear Mrs. Campos, I am familiar with 4375-20A>G (c.4243-20A>G) and think that it is likely a benign sequence change and, if no symptoms now, your baby does not have cystic fibrosis. Why? It is far within an intron (non-protein coding region) and it has been detected in 0.2% of 1990 NORMAL...
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