文献
J-GLOBAL ID:201702225311290929
整理番号:17A1174298
体GNAQ変異はスタージ・ウェーバー症候群における脳内皮細胞に豊富である【Powered by NICT】
Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome
著者 (11件):
Huang Lan
(Vascular Biology Program, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Huang Lan
(Department of Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Couto Javier A.
(Department of Plastic and Oral Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Pinto Anna
(Department of Neurology, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Alexandrescu Sanda
(Department of Pathology, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Madsen Joseph R.
(Department of Neurosurgery, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Greene Arin K.
(Department of Plastic and Oral Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Greene Arin K.
(Vascular Anomalies Center, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Sahin Mustafa
(Department of Neurology, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Bischoff Joyce
(Vascular Biology Program, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
,
Bischoff Joyce
(Department of Surgery, Boston Children’s Hospital and Harvard Medical School, Boston, Massachusetts)
資料名:
Pediatric Neurology
(Pediatric Neurology)
巻:
67
ページ:
59-63
発行年:
2017年
JST資料番号:
W3302A
ISSN:
0887-8994
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
オランダ (NLD)
言語:
英語 (EN)