De novo variants in RHOBTB2 ,...

Human Mutation 2018 / 05

De novo variants in RHOBTB2 , an atypical Rho GTPase gene, cause epileptic encephalopathy

Belal, Hazrat, Nakashima, Mitsuko, Matsumoto, Hiroshi, Yokochi, Kenji, Taniguchi-Ikeda, Mariko, Aoto, Kazushi, Amin, Mohammed Badrul, Maruyama, Azusa, Nagase, Hiroaki, Mizuguchi, Takeshi, Miyatake, Sa
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Language:
english
Journal:
Human Mutation
DOI:
10.1002/humu.23550
Date:
May, 2018
File:
PDF, 928 KB
english, 2018
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