Published in
Elsevier, Genetics in Medicine, 12(24), p. 2475-2486, 2022
DOI: 10.1016/j.gim.2022.09.002
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FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
Journal article published in 2022 by
Auriane Cospain 
,
Ana Rivera-Barahona,
Erwan Dumontet,
Blanca Gener,
Isabelle Bailleul-Forestier,
Isabelle Meyts,
Guillaume Jouret,
Bertrand Isidor,
Carole Brewer,
Wim Wuyts,
Leen Moens,
Selket Delafontaine ,
Wayne Wing Keung Lam,
Kris Van Den Bogaert,
Anneleen Boogaerts
and other authors.
,
Ana Rivera-Barahona,
Erwan Dumontet,
Blanca Gener,
Isabelle Bailleul-Forestier,
Isabelle Meyts,
Guillaume Jouret,
Bertrand Isidor,
Carole Brewer,
Wim Wuyts,
Leen Moens,
Selket Delafontaine ,
Wayne Wing Keung Lam,
Kris Van Den Bogaert,
Anneleen Boogaerts
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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