Role of Laparoscopy in Severe Gastrointestinal Bleeding Secondary to Coats Plus Syndrome
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Publisher
Springer Science and Business Media LLC
Reference10 articles.
1. Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects;Simon AJ;J Exp Med,2016
2. Functional characterization of human CTC1 mutations reveals novel mechanisms responsible for the pathogenesis of the telomere disease Coats plus;Gu P;Aging Cell,2013
3. Pathogenic CTC1 mutations cause global genome instabilities under replication stress;Wang Y;Nucleic Acids Res,2018
4. Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) or "Coats Plus": when peripheral retinal vasculature signals neurologic disease;Mansukhani S;J AAPOS,2017
5. Treatment of gastrointestinal bleeding in a probable case of cerebroretinal microangiopathy with calcifications and cysts;Briggs TA;Mol Syndromol,2011
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