文献
J-GLOBAL ID:202102222763421972
整理番号:21A0195773
MAMLD1変異体を有する個体における性発達の障害:WESとオリゴゲニック遺伝のインタラクトーム証拠【JST・京大機械翻訳】
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance
著者 (6件):
Li Lele
(Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing Children’s Hospital, The Capital Medical University, National Center for Children’s Health, Beijing, China)
,
Gao Fenqi
(Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing Children’s Hospital, The Capital Medical University, National Center for Children’s Health, Beijing, China)
,
Fan Lijun
(Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing Children’s Hospital, The Capital Medical University, National Center for Children’s Health, Beijing, China)
,
Su Chang
(Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing Children’s Hospital, The Capital Medical University, National Center for Children’s Health, Beijing, China)
,
Liang Xuejun
(Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing Children’s Hospital, The Capital Medical University, National Center for Children’s Health, Beijing, China)
,
Gong ChunXiu
(Department of Endocrinology, Genetics, Metabolism and Adolescent Medicine, Beijing Children’s Hospital, The Capital Medical University, National Center for Children’s Health, Beijing, China)
資料名:
Frontiers in Endocrinology (Web)
(Frontiers in Endocrinology (Web))
巻:
11
ページ:
582516
発行年:
2020年
JST資料番号:
U7068A
ISSN:
1664-2392
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
スイス (CHE)
言語:
英語 (EN)