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Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome.
Huang, Lan; Couto, Javier A; Pinto, Anna; Alexandrescu, Sanda; Madsen, Joseph R; Greene, Arin K; Sahin, Mustafa; Bischoff, Joyce.
Afiliação
  • Huang L; Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Couto JA; Department of Plastic and Oral Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Pinto A; Department of Neurology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Alexandrescu S; Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Madsen JR; Department of Neurosurgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Greene AK; Department of Plastic and Oral Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts; Vascular Anomalies Center, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Sahin M; Department of Neurology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Bischoff J; Vascular Biology Program, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts. Electronic address: joyce.bischoff@childrens.harvard.edu.
Pediatr Neurol ; 67: 59-63, 2017 02.
Article em En | MEDLINE | ID: mdl-27919468
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Síndrome de Sturge-Weber / Células Endoteliais / Subunidades alfa Gq-G11 de Proteínas de Ligação ao GTP Tipo de estudo: Prognostic_studies Limite: Child / Humans / Infant / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Síndrome de Sturge-Weber / Células Endoteliais / Subunidades alfa Gq-G11 de Proteínas de Ligação ao GTP Tipo de estudo: Prognostic_studies Limite: Child / Humans / Infant / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article