文献
J-GLOBAL ID:202002227732194121
整理番号:20A0524024
NPR2ミスセンス変異を伴うPHEX遺伝子変異により引き起こされた家族性低リン酸血症性くる病【JST・京大機械翻訳】
Familial hypophosphatemic rickets caused by a PHEX gene mutation accompanied by a NPR2 missense mutation
著者 (5件):
Zhao Yongting
(Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, P.R. China)
,
Yang Fan
(Department of Endocrinology, Drum Tower Hospital Affiliated to Nanjing University Medical School, Nanjing, China)
,
Wang Lihong
(Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, P.R. China)
,
Wang Lihong
(Translational Medicine Research and Cooperation Center of Northern China, Heilongjiang Academy of Medical Sciences, Harbin, China)
,
Che Hui
(Translational Medicine Research and Cooperation Center of Northern China, Heilongjiang Academy of Medical Sciences, Harbin, China)
資料名:
Journal of Pediatric Endocrinology and Metabolism
(Journal of Pediatric Endocrinology and Metabolism)
巻:
33
号:
2
ページ:
305-311
発行年:
2020年
JST資料番号:
W3758A
ISSN:
0334-018X
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
ドイツ (DEU)
言語:
英語 (EN)