TRIP12 mutations
Official Community
TRIP12 gene mutations have been reoccuringly identified in cohorts of individuals affected by neurodevelopmental complications. Phenotypic range is variable, but often includes speech impairment, autism, developmental delay and/or motor problems. This group would like to help connecting affected individuals, families and loved ones, as well as invested or interested science and healthcare professionals.
.png)
No hay comentarios:
Publicar un comentario