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1 Ergebnisse
1
KCNQ2 R144 variants cause neurodevelopmental disability wit..:
MICELI, Francesco
;
MILLEVERT, Charissa
;
SOLDOVIERI, Maria Virginia
...
2352-3964. , 2022
Link:
https://oskar-bordeaux.fr/handle/20.500.12278/183301
RT Journal T1
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism. ; EBioMedicine
UL https://suche.suub.uni-bremen.de/peid=base-ftoskarbordeaux:oai:oskar-bordeaux.fr:20.500.12278_183301&Exemplar=1&LAN=DE A1 MICELI, Francesco A1 MILLEVERT, Charissa A1 SOLDOVIERI, Maria Virginia A1 MOSCA, Ilaria A1 AMBROSINO, Paolo A1 CAROTENUTO, Lidia A1 SCHRADER, Dewi A1 LEE, Hyun Kyung A1 RIVIELLO, James A1 HONG, William A1 RISEN, Sarah A1 EMRICK, Lisa A1 AMIN, Hitha A1 VILLE, Dorothee A1 EDERY, Patrick A1 DE BELLESCIZE, Julitta A1 MICHAUD, Vincent A1 VAN-GILS, Julien A1 GOIZET, Cyril A1 WILLEMSEN, Marjolein H A1 KLEEFSTRA, Tjitske A1 MØLLER, Rikke S A1 DEVINSKY, Orrin A1 SANDS, Tristan A1 KORENKE, G Christoph A1 KLUGER, Gerhard A1 MEFFORD, Heather C A1 BRILSTRA, Eva A1 LESCA, Gaetan A1 MILH, Mathieu A1 COOPER, Edward C A1 WECKHUYSEN, Sarah YR 2022 K1 Amitriptyline K1 Autistic Disorder K1 Epilepsy K1 Gain of Function Mutation K1 Humans K1 Infant K1 Newborn K1 Diseases K1 KCNQ2 Potassium Channel K1 Language Development Disorders K1 Seizures K1 Sciences du Vivant [q-bio]/Génétique JF 2352-3964 LK http://dx.doi.org/https://oskar-bordeaux.fr/handle/20.500.12278/183301 DO https://oskar-bordeaux.fr/handle/20.500.12278/183301 SF ELIB - SuUB Bremen
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