Cargando…
Establishment of linkage phase, using Oxford Nanopore Technologies, for preimplantation genetic testing of Coffin-Lowry syndrome with a de novo RPS6KA3 mutation
Background: This study aimed to perform preimplantation genetic testing (PGT) for a female Coffin-Lowry Syndrome (CLS) patient with a de novo mutation (DNM) in RPS6KA3. It was challenging to establish the haplotype in this family because of the lack of information from affected family members. Hence...
Autores principales: | Wen, Xiaojun, Du, Jing, Li, Zhiming, Liu, Nengqing, Huo, Junye, Li, Jieliang, Ke, Wanna, Wu, Jiaqi, Fang, Xiaowu, Lin, Xiufeng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538565/ https://www.ncbi.nlm.nih.gov/pubmed/37779904 http://dx.doi.org/10.3389/fgene.2023.1169868 |
Ejemplares similares
-
Coffin-Lowry Syndrome Induced by RPS6KA3 Gene Variation in China: A Case Report in Twins
por: Jin, Huiying, et al.
Publicado: (2022) -
First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review
por: Song, Ari, et al.
Publicado: (2023) -
Coffin‐Lowry syndrome in a girl with 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 disruption by whole genome sequencing
por: Yamoto, Kaori, et al.
Publicado: (2020) -
Mechanical ventilation in Coffin-Lowry syndrome: a case
report
por: de Moura, Edmilson Bastos, et al.
Publicado: (2016) -
The natural history of spinal deformity in patients with Coffin-Lowry syndrome
por: Welborn, M., et al.
Publicado: (2018)