Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R.

Autor: Larasati, Yonika A.1 (AUTHOR) gonzalo.solis@unige.ch, Solis, Gonzalo P.1 (AUTHOR) alexey.koval@unige.ch, Koval, Alexey1 (AUTHOR), Griffiths, Silja T.2 (AUTHOR), Berentsen, Ragnhild3 (AUTHOR) ragnhild.drage.berentsen@helse-bergen.no, Aukrust, Ingvild3,4 (AUTHOR), Lesca, Gaetan5 (AUTHOR) gaetan.lesca@chu-lyon.fr, Chatron, Nicolas5 (AUTHOR) nicolas.chatron@chu-lyon.fr, Ville, Dorothée6 (AUTHOR) dorothee.ville@chu-lyon.fr, Korff, Christian M.7 (AUTHOR) christian.korff@hcuge.ch, Katanaev, Vladimir L.1,8 (AUTHOR) vladimir.katanaev@unige.ch
Zdroj: Cells (2073-4409). Oct2023, Vol. 12 Issue 20, p2469. 16p.
Databáze: Academic Search Ultimate
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