FOXP2 is the first gene to have been implicated in a developmental communication disorder. Is is said to play a prominent role in human cognition. When working properly FOXP2 is the regulator of the development of the neural pathways that underly both motor control and sensory-motor integration. The missense mutation is associated with a wide range of linguistic and grammatical deficits.

When you do this clearing your intention is to clear for all known or unknown mutations or anomalies of the FOXP2 gene.

ASSOCIATED FACTORS - Please do each of the following clearing separately to get the best results. Space these clearings out at least one-week apart from each other.

• Clear for resultant arginine-to-histidine substitution.within the DNA binding domain
• Clear for heterozygous missense mutations in FOXP2 - this may improve the sequencing of muscle movements used for speech. (This proved to be the case in one case study that’s presently active.)
• Clear for all known and unknown allelic variants of FOXP2 effecting speech and language function
• Clear for an non-functional FOXP2 exons.
• Restore the unmated FOXP2 protein sequence
• Clear for R328X and R553H mutations to stop the formation of FOXP2 protein lacking critical functional domains.
• Restore zinc finger and leucine zipper mediated dimerization

You may need to do a subsequent clearing for any collateral defects in FOXP1 and FOXP4

As you can see this is a pretty complicated clearing and you’ll probably need my help in doing this successfully. If you want to do this on your own I would make each one of the items in the bullet list above a separate Healing Intention Statement