FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects-Reference-Cited by-同舟云学术

FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects

Published:2022-12 Issue:12 Volume:24 Page:2475-2486
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Cospain Auriane^ORCID,Rivera-Barahona Ana,Dumontet Erwan,Gener Blanca,Bailleul-Forestier Isabelle,Meyts Isabelle,Jouret Guillaume,Isidor Bertrand,Brewer Carole,Wuyts Wim,Moens Leen,Delafontaine Selket,Keung Lam Wayne Wing,Van Den Bogaert Kris,Boogaerts Anneleen,Scalais Emmanuel,Besnard Thomas,Cogne Benjamin,Guissard Christophe,Rollier Paul,Carre Wilfrid,Bouvet Regis,Tarte Karin,Gómez-Carmona Ricardo,Lapunzina Pablo,Odent Sylvie,Faoucher Marie,Dubourg Christele,Ruiz-Pérez Víctor L.,Devriendt Koen,Pasquier Laurent,Pérez-Jurado Luis A.

Publisher

Elsevier BV

Subject

Genetics (clinical)

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