20EVALUATING GENETIC CAUSATION AND PERSONALIZED...

European Neuropsychopharmacology 2019 Vol. 29

20EVALUATING GENETIC CAUSATION AND PERSONALIZED PHARMACOLOGICAL TREATMENT OF AN ULTRA-RARE DISEASE ASSOCIATED WITH DELETION OF CACNG2

Kleiber, Morgan, Chapman, Timothy, Maile, M.L., Hong, O., Purcell, R., Lippa, A., Roberts, Amanda, Sebat, Jonathan
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Volume:
29
Year:
2019
Language:
english
Journal:
European Neuropsychopharmacology
DOI:
10.1016/j.euroneuro.2018.08.027
File:
PDF, 54 KB
english, 2019
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