Neurodevelopmental disorders linked to Aristaless homeobox gene: A 'fault disease model'

Autor: Padula, A., Poeta, L., Shoubridge, C., Valentino, M., Attianese, B., Vanbokhoven, H., Filosa, S., Gecz, J., Altucci, L., Miano, M.

Publikováno v: European journal of human genetics 26 (2018): 350–351.
info:cnr-pdr/source/autori:Padula, A.; Poeta, L.; Shoubridge, C.; Valentino, M.; Attianese, B.; vanBokhoven, H.; Filosa, S.; Gecz, J.; Altucci, L.; Miano, M./titolo:Neurodevelopmental disorders linked to Aristaless homeobox gene: A "fault disease model"/doi:/rivista:European journal of human genetics/anno:2018/pagina_da:350/pagina_a:351/intervallo_pagine:350–351/volume:26
Web of Science

Studying molecular convergence in neurodevelopmental disorders caused by mutations in specific disease-related genes permits us to define druggable molecular pathways. The purpose of our study is to assess the degree of damage associated with the ARX

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e554ae2801a141fc49e5dcdec2d21d01
http://www.cnr.it/prodotto/i/434892