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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.
Authors
E Ambrosini
Ms Brignone
+20Â more
L Catacuzzeno
D&apos
F Franciolini
A Grottesi
Renzo Guerrini
L Guglielmi
A Lanciotti
M Marchese
P Molinari
F Moro
C Napolitano
M. Pessia
S Pieroni
S Priori
Y Ruan
Fm Santorelli
I Servettini
G Servillo
F Sicca
G Valvo
Publication date
1 January 2014
Publisher
Abstract
Abstract is not available.
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Florence Research
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oai:flore.unifi.it:2158/987412
Last time updated on 17/04/2020