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Complex cerebrovascular diseases in Roberts syndrome caused by novel biallelic ESCO2 variations.
He, Shuang; Chen, Shuai; Li, Shu-Jian; Zhang, Jie-Wen; Liang, Xin-Liang.
Affiliation
  • He S; Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, 450003, China.
  • Chen S; Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, 450003, China.
  • Li SJ; Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, 450003, China.
  • Zhang JW; Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, 450003, China.
  • Liang XL; Department of Neurology, Zhengzhou University People's Hospital (Henan Provincial People's Hospital), Zhengzhou, Henan, 450003, China.
Mol Genet Genomic Med ; 11(6): e2177, 2023 06.
Article in En | MEDLINE | ID: mdl-37002187
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acetyltransferases / Chromosomal Proteins, Non-Histone / Cerebrovascular Disorders / Craniofacial Abnormalities Type of study: Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Mol Genet Genomic Med Year: 2023 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acetyltransferases / Chromosomal Proteins, Non-Histone / Cerebrovascular Disorders / Craniofacial Abnormalities Type of study: Prognostic_studies Limits: Adolescent / Female / Humans Language: En Journal: Mol Genet Genomic Med Year: 2023 Document type: Article Affiliation country: Country of publication: