Cargando…
Nonsense variants of STAG2 result in distinct congenital anomalies
Herein, we report two female cases with novel nonsense mutations of STAG2 at Xq25, encoding stromal antigen 2, a component of the cohesion complex. Exome analysis identified c.3097 C>T, p.(Arg1033*) in Case 1 (a fetus with multiple congenital anomalies) and c.2229 G>A, p.(Trp743*) in Case 2 (a...
Autores principales: | Aoi, Hiromi, Lei, Ming, Mizuguchi, Takeshi, Nishioka, Nobuko, Goto, Tomohide, Miyama, Sahoko, Suzuki, Toshifumi, Iwama, Kazuhiro, Uchiyama, Yuri, Mitsuhashi, Satomi, Itakura, Atsuo, Takeda, Satoru, Matsumoto, Naomichi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501222/ https://www.ncbi.nlm.nih.gov/pubmed/33014403 http://dx.doi.org/10.1038/s41439-020-00114-w |
Ejemplares similares
-
Retrospective Echocardiographic Analysis of West Syndrome During Adrenocorticotropic Hormone Therapy
por: Ikuta, Yoji, et al.
Publicado: (2022) -
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease
por: Tsuchida, Naomi, et al.
Publicado: (2019) -
Cervical Cerclage to Prevent Intrauterine Balloon Prolapse
por: Suzuki, Toshifumi, et al.
Publicado: (2023) -
Different NIPBL requirements of cohesin-STAG1 and cohesin-STAG2
por: Alonso-Gil, Dácil, et al.
Publicado: (2023) -
Respiratory Distress Syndrome in Infants Delivered via Cesarean from Mothers with Preterm Premature Rupture of Membranes: A Propensity Score Analysis
por: Nakahara, Mariko, et al.
Publicado: (2020)