文献
J-GLOBAL ID:202102284187233969
整理番号:21A0292655
21-ヒドロキシラーゼ欠乏による先天性副腎過形成患者の分子診断【JST・京大機械翻訳】
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
著者 (7件):
Reyes Tania Mayvel Espinosa
(National Institute of Endocrinology, Havana, Cuba)
,
Mesa Teresa Collazo
(National Institute of Endocrinology, Havana, Cuba)
,
Cruz Paulina Arasely Lantigua
(National Center for Medical Genetics, Havana, Cuba)
,
Machado Adriana Agramonte
(National Center for Medical Genetics, Havana, Cuba)
,
Alonso Emma Dominguez
(National Institute of Endocrinology, Havana, Cuba)
,
Falhammar Henrik
(Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden)
,
Falhammar Henrik
(Department of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital, Stockholm, Sweden)
資料名:
BMC Endocrine Disorders (Web)
(BMC Endocrine Disorders (Web))
巻:
20
号:
1
ページ:
1-8
発行年:
2020年
JST資料番号:
U7424A
ISSN:
1472-6823
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)