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Article

A novel mutation (insTCCG) in the TSC2 gene in a Chinese patient with tuberous sclerosis complex.

Journal of dermatological science - 1 Jan 2008

Yuan Cheng-Da, Chang Xiao-Li, Gao Min, Xiao Feng-Li, Wu Yao-Qun, Liu Qin, Shen Song-Ke, Liu Jun-Lin, Du Wen-Hui, Liu Jian-Jun, Yang Sen, Zhang Xue-Jun, Zhou Fu-Sheng, Fang Qiao-Yun

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17888633
DOI: 10.1016/j.jdermsci.2007.08.002

Genes

TSC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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A novel mutation (insTCCG) in the TSC2 gene in a Chinese patient with tuberous sclerosis complex.PMID 17888633Read ↗

A novel TSC2 mutation in a Chinese family with tuberous sclerosis complex.Semantic proximity Read ↗

A novel TSC2 mutation causing tuberless tuberous sclerosis.Semantic proximity Read ↗

A novel TSC2 mutation in a Korean patient with tuberous sclerosis complex.Semantic proximity Read ↗

Two novel TSC2 mutations in Chinese patients with tuberous sclerosis complex and a literature review of 20 patients reported in China.Semantic proximity Read ↗

Three novel mutations of TSC1 gene in Chinese patients with tuberous sclerosis complex.Semantic proximity Read ↗

A novel splice site mutation (156 + 1G-->A) in the TSC2 gene.Semantic proximity Read ↗

Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex.Semantic proximity Read ↗

A Chinese tuberous sclerosis complex family and a novel tuberous sclerosis complex-2 mutation.Semantic proximity Read ↗

A novel missense mutation in the GTPase activating protein homology region of TSC2 in two large families with tuberous sclerosis complexSemantic proximity Read ↗

[Identification of a novel TSC2 gene variant in a patient with tuberous sclerosis complex].Semantic proximity Read ↗

Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.Semantic proximity Read ↗

A novel de novo mutation in the TSC2 gene in a Chinese patient with tuberous sclerosis complex.Semantic proximity Read ↗

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