Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate.
J Hum Genet
; 64(7): 701-702, 2019 Jul.
Article
em En
| MEDLINE
| ID: mdl-31028281
ABSTRACT
Since the publication of this article, it has been brought to our attention, that the identified mutation (NM_015277 c.2617 G > A; p.Glu873Lys) is identical with the mutation (NM_001144967 c.2677 G > A; p.Glu893Lys) reported by Broix et al (Nature Genetics 48, 1349-1358, 2016 https//doi.org/10.1038/ng.3676 ). Therefore the mutation is not novel but recurrent. Accordingly, the word "novel" should be deleted throughout the article including the title. Thus, the title should read "A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate."
Texto completo:
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Base de dados:
MEDLINE
Idioma:
En
Revista:
J Hum Genet
Assunto da revista:
GENETICA MEDICA
Ano de publicação:
2019
Tipo de documento:
Article
País de afiliação:
Japão