Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphology - European Journal of Human Genetics European Journal of Human Genetics - Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphology

📢 Could truncating #SRRM1 variants be a hidden cause of neurodevelopmental disorders? 🧬🧠
#Genetics #Neurodevelopment #RareDisease

Read more ➡️ www.nature.com/articles/s41...