In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disruptingFOXP2

In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. Final version by Lottie D Morison & al. @ProfSimonFisher https://t.co/f1hfE6J6Ot

Interesting. Also another reason why I would like Zach seen my peadeatrics and genetics. Another referral done 🙈 see if they reject him AGAIN or 3rd time lucky 🙏

RT @MCRI_for_kids: A new paper from @MCRI_SpeechLang, published in @JMG_BMJ, has identified #FOXP2 as the primary gene to cause a severe sp…

RT @MCRI_for_kids: A new paper from @MCRI_SpeechLang, published in @JMG_BMJ, has identified #FOXP2 as the primary gene to cause a severe sp…