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Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease.
Ravindran, Ethiraj; Ullah, Noor; Mani, Shyamala; Chew, Elaine Guo Yan; Tandiono, Moses; Foo, Jia Nee; Khor, Chiea Chuen; Kaindl, Angela M; Siddiqi, Saima.
Afiliação
  • Ravindran E; Charité-Universitätsmedizin Berlin, Institute of Cell Biology and Neurobiology, Berlin, Germany.
  • Ullah N; Charité-Universitätsmedizin Berlin, Department of Pediatric Neurology, Berlin, Germany.
  • Mani S; Charité-Universitätsmedizin Berlin, Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Berlin, Germany.
  • Chew EGY; Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan.
  • Tandiono M; Khyber Medical University Institute of Paramedical Sciences (KMU IPMS), Peshawar, Pakistan.
  • Foo JN; Charité-Universitätsmedizin Berlin, Institute of Cell Biology and Neurobiology, Berlin, Germany.
  • Khor CC; Charité-Universitätsmedizin Berlin, Department of Pediatric Neurology, Berlin, Germany.
  • Kaindl AM; Charité-Universitätsmedizin Berlin, Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Berlin, Germany.
  • Siddiqi S; Human Genetics, Genome Institute of Singapore, ASTAR, Singapore, Singapore.
Front Neurol ; 13: 1017654, 2022.
Article em En | MEDLINE | ID: mdl-36341116
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article