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Mutations in KCNK4 that Affect Gating Cause a Recognizable ..:
Bauer, Christiane K
;
Calligari, Paolo
;
Radio, Francesca Clementina
...
info:eu-repo/semantics/altIdentifier/pmid/30290154. , 2018
Link:
http://hdl.handle.net/11573/1179916
RT Journal T1
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftunivromairis:oai:iris.uniroma1.it:11573_1179916&Exemplar=1&LAN=DE A1 Bauer, Christiane K A1 Calligari, Paolo A1 Radio, Francesca Clementina A1 Caputo, Viviana A1 Dentici, Maria Lisa A1 Falah, Nadia A1 High, Frances A1 Pantaleoni, Francesca A1 Barresi, Sabina A1 Ciolfi, Andrea A1 Pizzi, Simone A1 Bruselles, Alessandro A1 Person, Richard A1 Richards, Sarah A1 Cho, Megan T A1 Claps Sepulveda, Daniela J A1 Pro, Stefano A1 Battini, Roberta A1 Zampino, Giuseppe A1 Digilio, Maria Cristina A1 Bocchinfuso, Gianfranco A1 Dallapiccola, Bruno A1 Stella, Lorenzo A1 Tartaglia, Marco PB Cell Press; place:50 HAMPSHIRE ST, FLOOR 5, CAMBRIDGE, MA 02139 USA YR 2018 K1 channelopathy K1 epilepsy K1 FHEIG syndrome K1 gingival overgrowth K1 hypertrichosi K1 intellectual disability K1 K2P channel K1 neurodevelopmental disorder K1 TRAAK K1 Genetic K1 Genetics (clinical) JF info:eu-repo/semantics/altIdentifier/pmid/30290154 LK http://hdl.handle.net/11573/1179916 DO http://hdl.handle.net/11573/1179916 SF ELIB - SuUB Bremen
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