文献
J-GLOBAL ID:201902228956538258
整理番号:19A0713740
126家系におけるCBLC欠損の分子遺伝学的特性化およびメチルマロン酸尿症とホモシスチン尿症を合併した家系の出生前遺伝子診断【JST・京大機械翻訳】
Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria
著者 (4件):
Hu Shuang
(The Center for Genetics and Prenatal Diagnosis, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China)
,
Mei Shiyue
(The Center for Genetics and Prenatal Diagnosis, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China)
,
Liu Ning
(The Center for Genetics and Prenatal Diagnosis, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China)
,
Kong Xiangdong
(The Center for Genetics and Prenatal Diagnosis, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China)
資料名:
BMC Medical Genetics (Web)
(BMC Medical Genetics (Web))
巻:
19
号:
1
ページ:
154
発行年:
2018年
JST資料番号:
U7307A
ISSN:
1471-2350
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)