A novel HECW2 variant in an infant with congenital long QT syndrome

Pathogenic variants of HECW2 have been reported in cases of neurodevelopmental disorder with hypotonia, seizures, and absent language (NDHSAL; OMIM #617268). A novel HECW2 variant (NM_001348768.2:c.4343 T > C,p.Leu1448Ser) was identified in an NDHSAL infant with severe cardiac comorbidities. The...

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Detalles Bibliográficos
Autores principales: Imanishi, Rina, Nakau, Kouichi, Shimada, Sorachi, Oka, Hideharu, Takeguchi, Ryo, Tanaka, Ryosuke, Sugiyama, Tatsutoshi, Nii, Mitsumaro, Okamoto, Toshio, Nagaya, Ken, Makita, Yoshio, Yanagi, Kumiko, Kaname, Tadashi, Takahashi, Satoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244414/
https://www.ncbi.nlm.nih.gov/pubmed/37280227
http://dx.doi.org/10.1038/s41439-023-00245-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244414/
https://www.ncbi.nlm.nih.gov/pubmed/37280227
http://dx.doi.org/10.1038/s41439-023-00245-w

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