Literature DB >> 22040027

Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH.

Michela Barbaro, Fernanda C Soardi, Maricilda Palandi de Mello, Anna Wedell, Svetlana Lajic.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2012        PMID： 22040027     DOI： 10.1111/j.1365-2265.2011.04275.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN： 0300-0664            Impact factor:   3.478


× No keyword cloud information.
  2 in total

Review 1.  Management of congenital adrenal hyperplasia in childhood.

Authors:  Mimi S Kim; Anna Ryabets-Lienhard; Mitchell E Geffner
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2012-12       Impact factor: 3.243

2.  Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia.

Authors:  Ingeborg Brønstad; Lars Breivik; Paal Methlie; Anette S B Wolff; Eirik Bratland; Ingrid Nermoen; Kristian Løvås; Eystein S Husebye
Journal:  Endocr Connect       Date:  2014-04-15       Impact factor: 3.335
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.