PHOX2B polyalanine repeat mutation has a profound impact on the transcriptome of neuronal progenitor cells in Haddad syndrome
Tsering Stobdan, Vaishnavi Ventrapragada, Hang Ping Yao…·Gabriel G. Haddad
This study uses RNA-sequencing to show that PHOX2B polyalanine repeat mutation significantly alters the transcriptome of neuronal progenitor cells in Haddad syndrome.