Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 1(41), p. 69-80, 2019
DOI: 10.1002/humu.23915
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Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature
Journal article published in 2019 by
Claire Bar 
,
Giulia Barcia,
Mélanie Jennesson,
Gwenaël Le Guyader,
Amy Schneider,
Cyril Mignot,
Gaetan Lesca,
Delphine Breuillard,
Martino Montomoli,
Boris Keren,
Diane Doummar,
Thierry Billette de Villemeur,
Alexandra Afenjar,
Isabelle Marey,
Marion Gerard
and other authors.
,
Giulia Barcia,
Mélanie Jennesson,
Gwenaël Le Guyader,
Amy Schneider,
Cyril Mignot,
Gaetan Lesca,
Delphine Breuillard,
Martino Montomoli,
Boris Keren,
Diane Doummar,
Thierry Billette de Villemeur,
Alexandra Afenjar,
Isabelle Marey,
Marion Gerard
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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