The TSC2 c.2742+5G>A variant causes variable splicing changes and clinical manifestations in a family with tuberous sclerosis complex

BackgroundTuberous sclerosis complex (TSC) is a genetic, variably expressed, multisystem disease characterized by benign tumors. It is caused by pathogenic variants of the TSC complex subunit 1 gene (TSC1) and the TSC complex subunit 2 gene (TSC2). Genetic testing allows for early diagnosis, genetic...

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Bibliografische Detailangaben

Hauptverfasser:	Kuan Fan, Yi Guo, Zhi Song, Lamei Yuan, Wen Zheng, Xiao Hu, Lina Gong, Hao Deng
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Frontiers Media S.A. 2023-04-01
Schriftenreihe:	Frontiers in Molecular Neuroscience
Schlagworte:	tuberous sclerosis complex TSC2 gene splicing variant non-canonical splice site alternative splicing
Online-Zugang:	https://www.frontiersin.org/articles/10.3389/fnmol.2023.1091323/full
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