Cite
HARVARD Citation
Barone, R. et al. (2017). Familial 18q12.2 deletion supports the role of RNA‐binding protein CELF4 in autism spectrum disorders. American journal of medical genetics. 173 (6), pp. 1649-1655. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Barone, R. et al. (2017). Familial 18q12.2 deletion supports the role of RNA‐binding protein CELF4 in autism spectrum disorders. American journal of medical genetics. 173 (6), pp. 1649-1655. [Online].